U.S. flag

An official website of the United States government

NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.

Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2024.

Cover of GeneReviews®

GeneReviews® [Internet].

Show details

Familial Dysautonomia

Synonyms: Hereditary Sensory and Autonomic Neuropathy Type III (HSAN III), Riley-Day Syndrome

, MD.

Author Information and Affiliations

Initial Posting: ; Last Update: November 4, 2021.

Estimated reading time: 32 minutes

Summary

Clinical characteristics.

Familial dysautonomia, which affects the development and survival of sensory, sympathetic, and parasympathetic neurons, is a debilitating disorder present from birth. Neuronal degeneration progresses throughout life. Affected individuals have gastrointestinal dysfunction, autonomic crises (i.e., hypertensive vomiting attacks), recurrent pneumonia, altered pain sensitivity, altered temperature perception, and blood pressure instability. Hypotonia contributes to delay in acquisition of motor milestones. Optic neuropathy results in progressive vision loss. Older individuals often have a broad-based and ataxic gait that deteriorates over time. Developmental delay / intellectual disability occur in about 21% of individuals. Life expectancy is decreased.

Diagnosis/testing.

The diagnosis of familial dysautonomia is established in a proband with suggestive findings and biallelic pathogenic variants in ELP1 (formerly IKBKAP) identified by molecular genetic testing.

Management.

Treatment of manifestations: Affected individuals are often managed by multidisciplinary specialists that include neurologists, physiatrists, orthopedic surgeons, physical and occupational therapists, speech-language pathologists, pulmonologists, cardiologists, nephrologists, ophthalmologists, dentists and dental hygienists, and social workers. Feeding teams manage neurogenic dysphagia; mental health professionals treat anxiety.

Surveillance: Routine monitoring of the following: weight, nutrition, safety of oral feeding, developmental/educational progress, mental status, pulmonary function, sleep-disordered breathing, frequency and severity of dysautonomic crises, blood pressure lability, vision and low vision needs, ataxia and activities of daily living, spine for scoliosis, dental care and needs; assessment of caregiver needs.

Agents/circumstances to avoid: The following can exacerbate symptoms: hot or humid weather; full bladder.

Pregnancy management: Pregnancies in women with FD are considered high risk because of blood pressure lability. Visceral pain related to contractions during labor is perceived normally; therefore, analgesia should be provided.

Genetic counseling.

Familial dysautonomia is inherited in an autosomal recessive manner. If both parents are known to be heterozygous for an ELP1 pathogenic variant, each sib of an affected individual has at conception a 25% chance of being affected, a 50% chance of being an asymptomatic carrier, and a 25% chance of being unaffected and not a carrier. Once the ELP1 pathogenic variants have been identified in an affected family member, carrier testing for at-risk relatives, prenatal testing for a pregnancy at increased risk, and preimplantation genetic testing are possible. Carrier screening is available on a population basis for individuals of Ashkenazi Jewish heritage.

Diagnosis

The five cardinal clinical diagnostic criteria for familial dysautonomia are absence of fungiform papillae on the tongue, absence of flare after injection of intradermal histamine, decreased or absent deep-tendon reflexes, absence of overflow emotional tears, and Ashkenazi Jewish descent [Axelrod & Pearson 1984]. This last criterion, however, was rebutted after the discovery of three rare non-Jewish ELP1 variants [Leyne et al 2003].

Suggestive Findings

Clinical findings

  • Gastrointestinal dysfunction with vomiting crises
  • Recurrent aspiration pneumonia
  • Altered sensitivity to pain and temperature
  • Extreme blood pressure variability with postural hypotension
  • Hypotonia
  • Decreased or absent deep tendon reflexes
  • Decreased taste and absence of fungiform papillae of the tongue, giving it a smooth, pale appearance
  • Absence of overflow tears with emotional crying (alacrima) determined either by history in infants older than age three months or the Schirmer test (See Specialized testing.)

Specialized testing

  • Schirmer test. As newborns do not cry tears, the Schirmer test must be performed after age six months. In the Schirmer test, the end of a filter paper, 5 mm wide and 35 mm long, is placed in the lateral portion of a lower eyelid. Less than 10 mm of wetting of the filter paper after five minutes indicates diminished baseline and reflex tear secretion.
  • Absence of axon flare response after intradermal histamine injection
  • Pupillary hypersensitivity to parasympathomimetic agents. Topical administration of methacholine 2.5% or pilocarpine 0.0625% has no observable effect on the normal pupil but causes miosis after approximately 20 minutes in almost all individuals with FD.

Heritage. Infant is of Ashkenazi Jewish heritage. (Absence of known Ashkenazi Jewish heritage does not exclude the diagnosis.)

Establishing the Diagnosis

The diagnosis of familial dysautonomia is established in a proband with suggestive findings and biallelic pathogenic (or likely pathogenic) variants in ELP1 (formerly IKBKAP) identified by molecular genetic testing.

Note: (1) Per ACMG/AMP variant interpretation guidelines, the terms "pathogenic variants" and "likely pathogenic variants" are synonymous in a clinical setting, meaning that both are considered diagnostic and both can be used for clinical decision making [Richards et al 2015]. Reference to "pathogenic variants" in this section is understood to include any likely pathogenic variants. (2) Identification of biallelic ELP1 variants of uncertain significance (or identification of one known ELP1 pathogenic variant and one ELP1 variant of uncertain significance) does not establish or rule out the diagnosis.

Molecular genetic testing approaches can include a combination of gene-targeted testing (single-gene testing or multigene panel) and comprehensive genomic testing (exome sequencing, genome sequencing) depending on the phenotype.

Gene-targeted testing requires that the clinician determine which gene(s) are likely involved, whereas genomic testing does not. Individuals with the distinctive findings described in Suggestive Findings are more likely to be diagnosed using gene-targeted testing (see Option 1), whereas those in whom the diagnosis of familial dysautonomia has not been considered may be more likely to be diagnosed using genomic testing (see Option 2).

Option 1

Single-gene testing. Sequence analysis of ELP1 is performed first to detect small intragenic deletions/insertions and missense, nonsense, and splice site variants. Note: Depending on the sequencing method used, single-exon, multiexon, or whole-gene deletions/duplications may not be detected. Typically, if only one or no variant is detected by the sequencing method used, the next step is to perform gene-targeted deletion/duplication analysis to detect exon and whole-gene deletions or duplications; however, to date such variants have not been identified as a cause of this disorder.

In individuals of Ashkenazi Jewish heritage, targeted analysis for the ELP1 variant c.2204+6T>C (formerly IVS20+6T>C) can be performed first. This founder variant accounts for more than 99% of pathogenic variants among Ashkenazi Jewish individuals with FD.

A hereditary neuropathy multigene panel that includes ELP1 and other genes of interest (see Differential Diagnosis) is most likely to identify the genetic cause of the condition while limiting identification of variants of uncertain significance and pathogenic variants in genes that do not explain the underlying phenotype. Note: (1) The genes included in the panel and the diagnostic sensitivity of the testing used for each gene vary by laboratory and are likely to change over time. (2) Some multigene panels may include genes not associated with the condition discussed in this GeneReview. (3) In some laboratories, panel options may include a custom laboratory-designed panel and/or custom phenotype-focused exome analysis that includes genes specified by the clinician. (4) Methods used in a panel may include sequence analysis, deletion/duplication analysis, and/or other non-sequencing-based tests.

For an introduction to multigene panels click here. More detailed information for clinicians ordering genetic tests can be found here.

Option 2

When the diagnosis of familial dysautonomia has not been considered because an individual has atypical phenotypic features and/or is not known to have Ashkenazi Jewish heritage, comprehensive genomic testing, which does not require the clinician to determine which gene is likely involved, is the best option. Exome sequencing is most commonly used; genome sequencing is also possible.

For an introduction to comprehensive genomic testing click here. More detailed information for clinicians ordering genomic testing can be found here.

Table 1.

Molecular Genetic Testing Used in Familial Dysautonomia

Gene 1MethodProportion of Pathogenic Variants 2 Detectable by Method
ELP1 (IKBKAP)Targeted analysis for pathogenic variants 3>99% (Ashkenazi Jewish population) 4
Sequence analysis 5>99% 4
Deletion/duplication analysis 6None detected to date
1.
2.

See Molecular Genetics for information on variants detected in this gene.

3.

For pathogenic variants c.2204+6T>C and/or p.Arg696Pro [Dong et al 2002]

4.

Data derived from the subscription-based professional view of Human Gene Mutation Database [Stenson et al 2020]

5.

Sequence analysis detects variants that are benign, likely benign, of uncertain significance, likely pathogenic, or pathogenic. Variants may include small intragenic deletions/insertions and missense, nonsense, and splice site variants; typically, exon or whole-gene deletions/duplications are not detected. For issues to consider in interpretation of sequence analysis results, click here.

6.

Gene-targeted deletion/duplication analysis detects intragenic deletions or duplications. Methods used may include quantitative PCR, long-range PCR, multiplex ligation-dependent probe amplification (MLPA), and a gene-targeted microarray designed to detect single-exon deletions or duplications.

Clinical Characteristics

Clinical Description

Familial dysautonomia (FD) affects the development and survival of sensory, sympathetic, and parasympathetic neurons. It is a debilitating disease present from birth. Neuronal degeneration progresses throughout life. Affected individuals have gastrointestinal dysfunction, autonomic crises (I.e., hypertensive vomiting attacks), recurrent pneumonia, altered pain sensitivity, altered temperature perception, and cardiovascular instability. Hypotonia contributes to delay in acquisition of motor milestones. Older individuals often have a broad-based and ataxic gait that deteriorates over time. Developmental delay / intellectual disability occur in about 21% of individuals. Life expectancy is decreased [Welton et al 1979].

Table 2.

Clinical Manifestations of Familial Dysautonomia

System
Involved		Clinical Manifestations
Autonomic
system
  • Oropharyngeal incoordination (60% of neonates)
  • Esophageal dysmotility, GERD 1
  • Insensitivity to hypercapnia and hypoxia 2
  • Breath holding
  • Orthostatic hypotension w/o compensatory tachycardia 1, 3
  • Supine hypertension 1
  • Autonomic crises (i.e., hypertensive vomiting attacks) (40%)
Sensory
system
  • Insensitivity to pain (sparing hands, soles of feet, neck, & genital areas) 1
  • Abnormal temperature perception on trunk & lower extremities 1
  • Depressed patellar reflexes
Motor
system
  • Hypotonia
  • Mild/moderate motor DD
  • Broad-based or mildly ataxic gait 1
  • Spinal curvature (95%; esp kyphosis) 1
Cranial
nerves
  • Absence of overflow tears
  • Depressed corneal reflexes
  • Optic nerve atrophy 1
  • Strabismus
  • Deficient taste, esp sweet
  • Dysarthric, nasal speech
Respiratory 4
  • Chronic aspiration & recurrent aspiration pneumonia
  • Suppurative lung disease & bronchiectasis
  • Restrictive lung disease
  • Upper-airway obstruction due to cranial dimorphism & ↓ muscle tone of pharyngeal muscles, → obstructive sleep apnea
  • Obstructive lung disease & airway hyperreactivity
  • Sleep-disordered breathing (obstructive & central sleep apnea)
  • Daytime hypoventilation
Renal 5
  • CKD w/histopathologic features of chronic hypertensive nephrosclerosis
  • Tubular atrophy
  • Lack of sympathetic innervation of renal vasculature
  • ↑ incidence of rare kidney malformations & hydronephrosis
Cognitive
ability /
Personality
  • Usually normal intellect (verbal skills better than motor)
  • Concrete or literal thinking
  • Skin picking (esp fingers & nose)
  • Resistance to change (phobias) 1

Adapted from Axelrod [1996]

CKD = chronic kidney disease; DD = developmental delay; GERD = gastroesophageal reflux disease

1.

Progressive neurologic abnormalities

2.
3.
4.
5.

Most infants with familial dysautonomia are born after an uncomplicated term pregnancy. However, there is an increased rate of polyhydramnios and breech presentation.

Autonomic dysfunction. Neonates (i.e., infants age ≤28 days) typically have impaired oropharyngeal incoordination (i.e., neurogenic dysphagia) manifest as poor initiation of sucking and poor swallowing mechanisms. Protective airway reflexes (including cough) are decreased or lacking; the risk of aspiration and aspiration pneumonia shortly after birth is extremely high. Additional gastrointestinal problems that can interfere with eating and weight gain include esophageal dysmotility and GERD.

Infants with FD may have difficulties maintaining normal body temperature and may be indifferent to pain stimuli.

Sympathetic nervous system involvement results in orthostatic hypotension that is exacerbated by exercise and warm environments. Syncope is surprisingly infrequent, and usually indicates volume depletion, anemia, or hypoxia.

Urinary stress incontinence is common in adolescent and adult women [Saini et al 2003].

Episodic somnolence has been reported.

Autonomic crises, also described as hypertensive vomiting attacks, occur in about 40% of individuals. Attacks occur when stimuli increase sympathetic outflow causing an uncontrolled release of catecholamines (neurotransmitters such as epinephrine and dopamine) into the circulation. Common triggers include emotion, illness, abdominal discomfort, and bladder distension; however, sometimes the crises are unpredictable and without obvious cause. Dopamine, which is believed to activate receptors in the chemoreceptor trigger zone of the area postrema (located in the medulla oblongata), cause cyclic vomiting (or retching in persons who have undergone fundoplication). These dopaminergic crises can also be associated with tachycardia, hyperhidrosis, irritability, and personality changes. Crises may last several days.

Sensory disturbances are significant. Pain and temperature thresholds are greatly elevated; affected individuals report a relative indifference to pain. The risk for decubitus ulcers, burns, and other minor injuries to become infected is increased. Failure to recognize fractures has also been described.

Motor development. Infants and young children have varying degrees of hypotonia that contribute to delay in motor milestones. Although some infants may acquire motor skills in the usual timeframe, most infants demonstrate some degree of delay in acquisition of motor skills. Sitting without support is usually achieved around age 12-18 months, standing alone around age one to two years, and walking independently around age two to three years [Sheba Medical Center Familial Dysautonomia Database, unpublished data].

Older individuals often have a broad-based, ataxic gait that progressively deteriorates over time. Individuals with FD have difficulty performing rapid movements and maintaining their balance while changing direction or turning. By age 20 years 3% of affected individuals require assistance walking; this percentage increases linearly to 14% by age 30 years, 27% by age 40 years, and 49% by age 50 years [Macefield et al 2011].

Ophthalmologic. Recurrent corneal ulcers and occasionally permanent opacities result from alacrima and corneal hypoesthesia.

The major cause of visual loss in FD is optic neuropathy affecting mostly the P-type retinal ganglion cells. Beginning early in life, all individuals with FD experience progressive loss of retinal ganglion cell axons. The temporal retinal nerve fiber layer (RNFL) is the most affected. The less energy-dependent ganglion cells are relatively spared, whereas the more energy-dependent maculopapillary ganglion cells are selectively damaged [Mendoza-Santiesteban et al 2014]. The accelerated retinal damage continues until the third decade of life and then plateaus [Kfir et al 2021]. Visual impairment frequently begins at an early age and can progress to blindness usually after the third decade of life.

Eye movement disorders such as strabismus are very common.

Respiratory illness is common. According to the New York University Familial Dysautonomia Patient Registry [Kazachkov et al 2018], upper-airway obstruction is present in 83%, lower-airway disease in 85%, and restrictive lung disease in 94% [Palma et al 2019].

Although most individuals undergo gastrostomy with Nissen fundoplication upon diagnosis, recurrent lower-airway infections remain common. Most individuals with FD develop chronic lung disease secondary to recurrent aspiration. CT imaging of the lungs shows bronchiectasis in 26% of affected individuals.

Lack of input from the peripheral chemoreceptors results in almost absent ventilatory responses to hypoxemia; the chemoreceptor ventilatory responses to hypercapnia are also reduced, but to a lesser extent.

The majority of children and adults with FD have some degree of sleep-disordered breathing. Central apnea is more frequent in children; obstructive apnea is more frequent in adults.

The increased incidence of sudden death during sleep can be attributed to the following risk factors: treatment with fludrocortisone, plasma potassium concentrations <4 mEq/L, and untreated sleep apnea [Palma et al 2017].

Kyphoscoliosis, a common finding, develops during the first two decades. By age 20 years, 80% of affected individuals have some degree of spinal deformity, possibly due to abnormal posture of the trunk as needed to maintain balance.

Renal. Chronic kidney disease is common. Renal function tends to deteriorate with advancing age. Almost all persons with FD who reach their fourth decade have a markedly decreased estimated glomerular filtration rate (eGFR) [Elkayam et al 2006].

Baroreflex failure, manifest as excessive increases or decreases in blood pressure with wide fluctuations, is associated with a faster progression of renal disease. Some individuals progress to end-stage renal disease and may require dialysis. A few renal transplants have been performed.

Renal tubular acidosis, requiring treatment, is common. Hyperkalemia, which is also common, is not always explained by the degree of renal insufficiency.

There is also an increased incidence of congenital renal defects, including a single kidney, horseshoe kidney, and crossed renal ectopia (i.e., a kidney that has crossed from its side to the other side such that the kidneys are both located on one side of the body) [Norcliffe-Kaufmann et al 2013a].

Cognitive function differs widely among affected individuals. Both learning difficulties and poor concentration are common. Although acquisition of verbal skills is delayed during the first nine years, verbal skills subsequently improve to within the normal range for age [Palma et al 2014].

Personality issues. Anxiety is the most common psychiatric problem. Skin or nail picking and trichotillomania occur in around 10% of individuals [Palma et al 2014].

Other

  • Craniofacial findings include small jaw, mandibular retrognathia, malocclusion, dental crowding, and smaller tooth size [Mass 2016].
  • Dental trauma occurs in 60% of individuals (often from frequent falling due to ataxia and balance issues); 32% have orodental self-mutilation (i.e., chewing the gums without noticing).
  • Sexual maturation is frequently delayed; however, sexual development is normal in both sexes. Women with FD have delivered normal infants following uncomplicated pregnancies. Fertility in males has been reported; one male has fathered six children.
  • Growth. Neonates with FD are usually born appropriate for gestational age with head circumference within the normal range. Individuals with FD often fall severely below their projected midparental adjusted height; the reported average adult height for males is 158 centimeters and for females is 150 centimeters.
    Although poor linear growth velocity, low-to-normal insulin-like growth factor-I (IGFI) levels, and delayed skeletal age are reported in FD, challenge tests for growth hormone deficiency have been inconclusive. Growth hormone treatment in individuals in an open-label study resulted in growth velocity that exceeded pre-treatment rates in 12 of the 13 treated individuals [Kamboj et al 2004].

Quality of life. Using a questionnaire to evaluate the quality of life in persons with FD, Sands et al [2006] determined that FD imposed a greater physical than psychosocial burden on children, whereas young adults reported both mental and physical quality of life within the average range. Self-esteem was problematic and improved with age. Both age groups reported decreasing physical quality of life with age, with worsening general health that limited their roles at school or work.

Prognosis. FD has always been recognized as a potentially life-threatening disorder with a high mortality rate and a high incidence of sudden death. Causes of death are primarily pulmonary (26%) and unexplained (38%); the latter may result from unopposed vagal stimulation. Sepsis is also a significant cause of death (11%) [Axelrod et al 2002].

Genotype-Phenotype Correlations

No genotype-phenotype correlations have been observed [Blumenfeld et al 1999].

The p.Arg696Pro pathogenic variant is extremely rare in the Ashkenazi Jewish population and has never been detected in the homozygous state; therefore, the phenotype associated with p.Arg696Pro homozygosity is unknown.

Prevalence

The incidence of FD among the Ashkenazim is 1:3,700 live births, which corresponds to a carrier frequency of 1:36 [Slaugenhaupt et al 2001].

A study by Lehavi et al [2003] from Israel identified 34 carriers among 1100 individuals of full Ashkenazi Jewish parentage (carrier rate 1:32). Further analysis revealed different carrier frequencies among a subset of Polish Ashkenazi Jews: Among the 195 individuals of full Polish background, 11 carriers were detected (1:18), in contrast to only three of the 298 of full non-Polish background (1:99).

Differential Diagnosis

Table 3.

Genes and Disorders of Interest in the Differential Diagnosis

Gene(s)DisorderMOIClinical Characteristics / Comment
ATL1 HSN1D (See Spastic Paraplegia 3A.)ADLoss of pain & temperature sensation; osteomyelitis; lancinating pain; distal motor involvement (variable); facultative deafness; no visceral signs of autonomic involvement
ATL3 HSN1F (OMIM 615632)AD
  • Loss of pain & temperature sensation; osteomyelitis; lancinating pain; distal motor involvement (variable); facultative deafness; no visceral signs of autonomic involvement
  • Similar to HSN1D 1
CLTCL1
NGF
NTRK1
PRDM12
SCN9A
SCN11A
ZFHX2 		Congenital insensitivity to pain (See also NTRK1 Congenital Insensitivity to Pain with Anhidrosis.)AR
AD
  • Inability to perceive pain from birth from any noxious stimuli leading to repeated injuries & prevention of normal healing. Painless fractures & joint damage frequently occur & can lead to permanent damage; corneal injuries; anhidrosis that disturbs thermoregulation & can lead to recurrent episodes of unexplained fever (Note: marked hyperhidrosis is observed in assoc w/SCN11A c.2432T>C [p.Leu811Pro].)
  • Self-mutilating injuries of the fingers (biting off fingertips) & oral cavity (incl loss of the tongue tip, injuries to the inside of the teeth/gums, & avulsion of teeth) are common.
DNMT1 HSN1E AD
  • Loss of pain & temperature sensation; osteomyelitis; lancinating pain; distal motor involvement (variable); facultative deafness; no visceral signs of autonomic involvement
  • Distinguished by hearing loss, dementia, & narcolepsy
DST HSAN6 (OMIM 614653)ARDysautonomic symptoms; absent tearing, feeding difficulties, absent deep tendon reflexes, abnormal histamine test w/no axon flare, distal contractures, motionless open-mouthed facies, severe ID/DD, early death -2
KIF1A
RETREG1
SCN9A
WNK1 		HSAN2 ARProgressively ↓ sensation to pain, temperature, & touch. Onset can be at birth & is often before puberty. Sensory deficit is predominantly distal (lower limbs more severely affected than upper limbs). Over time sensory function becomes severely ↓. Unnoticed injuries & neuropathic skin promote ulcerations & infections → spontaneous amputation of digits or need for surgical amputation. Osteomyelitis is common. Painless fractures can complicate the disease. Autonomic disturbances are variable.
LIFR Stüve-Wiedemann syndrome (OMIM 601559)ARCombination of autonomic nervous system manifestations resembling FD & characteristic bony changes (bowing of long bones, camptodactyly) 3
MPZ CMT2IJ (See CMT Overview.)ADp.Thr124Met is assoc w/severe sensory loss, shooting pains, & occasional pseudo-Argyl-Robertson pupils but no ulcerations.
RAB7A CMT2B (See CMT Overview.)AD
  • Acral ulcero-mutilating sensory neuropathy; sensory loss of all modalities w/a high frequency of foot ulcers necessitating amputations
  • Motor features are common; distal muscle weakness & wasting are often the 1st & most prominent features.4
SPTLC1 HSAN1A ADProminent early sensory loss & later positive sensory phenomena (e.g., dysesthesia & characteristic "lightning" or "shooting" pains); painless injuries, which, if unrecognized, result in slow wound healing & subsequent osteomyelitis requiring distal amputations; motor involvement is present in all advanced cases & can be severe; SNHL is variable; onset ranges from teens to 6th decade.
SPTLC2 HSAN1CADPhenotypically similar to HSAN1A
TECPR2 TECPR2-related HSAN with ID ARDD/ID, muscular hypotonia, ataxia, hyporeflexia, respiratory infections, & central/nocturnal hypopnea

AD = autosomal dominant; AR = autosomal recessive; DD = developmental delay; FD = familial dysautonomia; HSAN = hereditary sensory and autonomic neuropathy; ID = intellectual disability; MOI = mode of inheritance; SNHL = sensorineural hearing loss; XL = X-linked

1.
2.

Only one affected family has been reported to date [Edvardson et al 2012].

3.
4.

HSAN1B (OMIM 608088), a disorder of unknown genetic cause, can also be considered in the differential diagnosis. HSAN1B is characterized by cough and gastroesophageal reflux; loss of pain & temperature sensation; osteomyelitis; lancinating pain; distal motor involvement (variable); and facultative deafness. There are no visceral signs of autonomic involvement.

Management

Clinical practice guidelines have been published [Kazachkov et al 2018] (full text).

Evaluations Following Initial Diagnosis

To establish the extent of disease and needs in an individual diagnosed with familial dysautonomia, the evaluations summarized in Table 4 (if not performed as part of the evaluation that led to the diagnosis) are recommended.

Table 4.

Recommended Evaluations Following Initial Diagnosis in Individuals with Familial Dysautonomia

System/ConcernEvaluationComment
Growth Measure height, weight, head circumference
Neurologic involvement By pediatric neurologist
  • Comprehensive neurologic exam w/attn to sensory ataxia, abnormalities in proprioception
  • Positive Romberg sign; ↓ or absent deep tendon & H-reflexes
  • Consider: (1) MRI if concerns re worsening gait ataxia &/or balance; (2) EEG if concerns re seizures.
Development Developmental assessment for infants/young children
  • To incl motor, adaptive, & cognitive eval
  • Eval by speech-language pathologist
  • Eval for early childhood intervention programs / special education
Cognitive abilities Standardized testing
Psychiatric/behavioral
issues 		Assessment by mental health professional as neededAnxiety is the most common psychiatric problem.
Neurogenic dysphagia Multidisciplinary incl pulmonologist, neurologist, nutritionist, gastroenterologist, speech-language pathologist, chest physiotherapist, & caregiversBaseline eval by multidisciplinary team w/video fluoroscopic swallow study to define safe consistencies of food & best oral hygiene
Blood pressure
instability 		24-hr blood pressure monitoring & orthostatic challenge
Decreased sensitivity
to pain 		Skin examFor decubitus ulcers & pressure sores (e.g., from shoes & devices such as back brace)
Sleep-disordered breathing Full (in-laboratory) polysomnography incl end-tidal CO2 measurementsPerform even if no clinical manifestations. Transcutaneous CO2 measurements may be unreliable.
Airway
disease 		Upper-airway
obstruction 		Laryngoscopy, sleep endoscopyPerform awake flexible laryngoscopy when breathing is noisy. If no anatomic obstruction is found, consider sleep laryngoscopy.
Lower-airway
disease 		Pulmonary function tests, sputum cultures, bronchoscopy, & bronchoalveolar lavage
  • Spirometry & response to bronchodilators may help assess airway obstruction.
  • Obtain culture from lower airways when clinical evidence suggests suppurative lung disease.
Restrictive
lung disease 		Lung volume measurements via plethysmography or nitrogen washoutSecondary to hyperkyphotic (usually upper thoracic) scoliosis, mostly during 2nd decade
Acute
respiratory
exacerbation 		Respiratory exam & chest x-ray
  • Acute respiratory exacerbation may present w/minimal symptoms despite significant hypoxemia & hypercarbia; because respiratory drive remains depressed even during acute respiratory exacerbations, patients do not appear dyspneic or tachypneic.
  • Dysautonomic crises may occur during acute respiratory exacerbations & are often the presenting manifestation.
Dysautonomic crises As determined by medical historyHyperadrenergic vomiting attacks may continue for several days.
Ophthalmologic
involvement 		Ophthalmologic exam
  • Incl assessment of best corrected visual acuity, cornea for possible injury due to ↓ corneal sensation, fundoscopic exam for evidence of optic atrophy.
  • Assessment of retina to incl OCT w/measurements of mean RNFL & macular GCIPL thickness
Musculoskeletal Physical medicine & rehab / PT / OT evalTo incl assessment of:
  • Gross motor & fine motor skills & need for PT (to improve gross motor skills) &/or OT (to improve fine motor skills)
  • Need for AFOs, specialized shoes
  • Mobility, activities of daily living, & need for adaptive devices/durable equipment
Eval by pediatric orthopedistAssess amount & progression of spinal curvature & extent of foot deformities.
Dental Eval by dental hygienist
  • ↑ saliva flow may ↓ incidence of dental caries, but changes in composition of saliva → more plaque & ↑ in periodontal disease.
  • Evaluate for dental, gingival, & tongue trauma (usually due to self-mutilation).
General dental evalEvaluate for dental, gingival, & tongue trauma (usually due to self-mutilation).
Eval by orthodontists & maxillofacial professionalsTo assess abnormalities of bite & dental spacing
Genetic counseling By genetics professionals 1To inform affected persons & their families re nature, MOI, & implications of FD in order to facilitate medical & personal decision making
Family support &
resources 		Assess:

AFO = ankle/foot orthoses; FD = familial dysautonomia; GCIPL = ganglion cell and inner plexiform layer; MOI = mode of inheritance; OCT = optic coherence tomography; RNFL = retinal nerve fiber layer

1.

Medical geneticist, certified genetic counselor, certified advanced genetic nurse

Treatment of Manifestations

There is no curative therapy for familial dysautonomia. Treatment is supportive.

Affected individuals are often managed by a multidisciplinary team that includes neurologists, physiatrists, orthopedic surgeons, physical and occupational therapists, speech-language pathologists, pulmonologists, and social workers (see Table 5).

Table 5.

Treatment of Manifestations in Individuals with Familial Dysautonomia

Manifestation/ConcernTreatmentConsiderations/Other
Short stature Growth hormone treatment may be effective & should be considered based on guidelines re height, growth velocity, & bone maturation. 1
  • GH stimulation testing may not be reliable.
  • Monitor spinal curvature, as it tends to worsen during accelerated growth.
Neurogenic dysphagia Per feeding team; for infants, thickened formula & different-shaped nipples to manage oropharyngeal incoordinationLow threshold for gastrostomy tube & Nissen fundoplication to maintain nutritional status & ↓ risk of aspiration
GERD Upright positioning w/feeds, prokinetic agents, H2 antagonists, proton pump inhibitors, & gastrostomy w/or w/o fundoplication are appropriate.A diagnosis of GERD should be confirmed w/esophageal impedance & manometry.
DD / Educational issues See Developmental Delay / Intellectual Disability Management Issues.
Psychiatric/behavioral
issues 		By mental health professionalSelective serotonin reuptake inhibitors are sometimes effective in treating anxiety; psychotherapy & behavioral techniques may also help.
Blood pressure
instability 		Carbidopa is effective in reducing blood pressure variability. 2
Decreased sensitivity
to pain 		Close attn to decubitus ulcers, burns, & other minor injuries, joint swelling & bone deformity. Signs of local or systemic infection should be monitored & treated w/antibiotics.
Sleep-disordered
breathing 		CPAP or BiPAPDue to chemoreflex failure, begin noninvasive ventilation even when sleep-disordered breathing is mild to ↓ risk of sudden unexpected death during sleep. 3
Airway
disease 		Upper-airway
obstruction 		Tonsillectomy & adenoidectomy.If upper-airway obstruction is not resolved, refer to airway mgmt specialist.
Lower-airway
disease 		Treat suppurative lung disease/bronchiectasis w/daily chest physiotherapy.
  • Cough augmentation is most effective in clearing airway mucus & best achieved by mechanical insufflation/exsufflation methods.
  • Inhaled hypertonic saline may be beneficial.
  • Treat acute exacerbation promptly w/antibiotics.
Restrictive
lung disease 		Airway mucus clearance w/manually assisted coughing or mechanical insufflation/exsufflation methodsConsider surgical correction of scoliosis on a case-by-case basis. Surgical complications can be severe; data re respiratory function pre- & post-surgery are lacking.
Acute
respiratory
exacerbation 		Start antibiotics covering aspiration flora promptly, preferably after obtaining sputum culture.
  • Oral antibiotics for 14 days
  • Initiation of IV antibiotics depends on baseline respiratory status; consider when no improvement after oral antibiotics.
Chronic lung
disease 		Daily chest physiotherapy (nebulization, bronchodilators, cough augmentation, incentive spirometry, & postural drainage)
  • Early diagnosis & treatment of pneumonia & infections (secondary to aspiration)
  • Treatment w/oseltamivir is indicated for influenza virus infections. 4
Dysautonomic crises
  • Instructions to manage crises at home w/fluids & medications via gastrostomy
  • Guidance re when to visit ER for more extensive eval & treatment
Careful attn to dehydration & electrolyte imbalance; investigate underlying cause when crises are refractory to treatment or other symptoms are present.
Benzodiazepines ↓ retching/vomiting. As ventilation may be suppressed, noninvasive ventilation is recommended as a precaution.IV benzodiazepine may cause prolonged apnea & should only be administered in ER or ICU settings.
Clonidine (centrally acting α2-adrenergic agonist) may ↓ sympathetic activity.May be given via gastrostomy, sublingually, or transdermally
Intranasal dexmedetomidine may be a feasible & safe acute treatment for adrenergic crisis. 5In severe cases IV dexmedetomidine may be used, but only in ICU settings. 6
Carbidopa (dopa-decarboxylase inhibitor) given daily may ↓ frequency & severity of hypertensive vomiting attacks. 7
Bradyarrhythmia PacemakerFor those w/history of syncope &/or cardiac arrest
Orthostatic
hypotension
  • Physical countermaneuvers to ↑ venous return & PT to ↑ muscle strength in legs help prevent orthostatic hypotension.
  • Treatment w/midodrine may be effective for short periods; use as needed prior to physical activity that may cause orthostatic hypotension.
  • Hydration is useful only for short periods due to impaired osmopressor response (most likely due to ↓ function of peripheral osmosensory pathway).
Treatment of orthostatic hypotension w/high doses of fludrocortisone aggravates renal damage.
Hypertension Attn to factors precipitating hypertension (rather than use of antihypertensive agents) as blood pressure is labileSleeping w/20°-40° elevation of head of bed ↓s supine hypertension & nocturnal pressure-diuresis & ↑s intravascular volume in the AM.
Standard treatment of hypertension in persons w/CKD
Kidney
  • Adequate control of blood pressure
  • Treat renal tubular acidosis w/bicarbonate.
  • Low-potassium diet for hyperkalemia
Ophthal-
mologic 		Optic
neuropathy 		Low vision aidsPer low vision clinic
Corneal
ulceration 		Artificial tear solutions (w/methylcellulose) 3-6x/day, maintenance of normal body hydration, & moisture chamber spectacle attachments
  • Soft contact lenses can promote healing.
  • Tarsorrhaphy only for corneal injury unresponsive to routine measures
  • Corneal transplantation offers limited success.
Chronic
blepharitis 		Combined topical antibiotic/corticosteroid ointment
Strabismus Early surgical correction may help.
Sensory ataxia OT/PTMany adults use walkers or wheelchairs when outside the home.
Musculo-
skeletal 		Foot
deformity 		PT to preserve flexibility; special shoes w/good ankle support &/or AFOs to correct foot drop & aid walkingExcellent ongoing foot care to avoid development of ulcers at pressure points
Spine
deformities 		PT to preserve flexibilityBracing is not effective & may cause pressure ulcers; spinal fusion may be necessary.
Dental Sialorrhea Botulinum toxin injections in major salivary glandsSurgical approaches & anticholinergic drugs were used in the past.
Excessive
plaque &
calculus
accumulation 		Dental cleaning & preventive careBiannually by dental hygienist
Periodontal
disease, dental
trauma, & self-
mutilation 		Dental eval & careAssess for occult biting of oral mucosa & establish plan for tooth extraction when needed.
Small jaw Care by maxillofacial professionalsAs needed for dental crowding & moderate/severe malocclusion
Family support &
resources 		Address caregiver needs (e.g., respite care, home nursing, coordination of multiple subspecialty appointments, equipment, medications, & supplies).

AFOs = ankle/foot orthoses; BiPAP = bi-level positive airway pressure; CKD = chronic kidney disease; CPAP = continuous positive airway pressure; GERD = gastroesophageal reflux disease; OT = occupational therapy; PT = physical therapy

1.
2.
3.
4.
5.
6.
7.

Developmental Delay / Intellectual Disability Management Issues

The following information represents typical management recommendations for individuals with developmental delay / intellectual disability in the United States; standard recommendations may vary from country to country.

Ages 0-3 years. Referral to an early intervention program is recommended for access to occupational, physical, speech, and feeding therapy as well as infant mental health services, special educators, and sensory impairment specialists. In the US, early intervention is a federally funded program available in all states that provides in-home services to target individual therapy needs.

Ages 3-5 years. In the US, developmental preschool through the local public school district is recommended. Before placement, an evaluation is made to determine needed services and therapies and an individualized education plan (IEP) is developed for those who qualify based on established motor, language, social, or cognitive delay. The early intervention program typically assists with this transition. Developmental preschool is center based; for children too medically unstable to attend, home-based services are provided.

All ages. Consultation with a developmental pediatrician is recommended to ensure the involvement of appropriate community, state, and educational agencies (US) and to support parents in maximizing quality of life. Some issues to consider:

  • Individualized education plan (IEP) services:
    • An IEP provides specially designed instruction and related services to children who qualify.
    • IEP services will be reviewed annually to determine whether any changes are needed.
    • Special education law requires that children participating in an IEP be in the least restrictive environment feasible at school and included in general education as much as possible, when and where appropriate.
    • Vision and hearing consultants should be a part of the child's IEP team to support access to academic material.
    • PT, OT, and speech services will be provided in the IEP to the extent that the need affects the child's access to academic material. Beyond that, private supportive therapies based on the affected individual's needs may be considered. Specific recommendations regarding type of therapy can be made by a developmental pediatrician.
    • As a child enters the teen years, a transition plan should be discussed and incorporated in the IEP. For those receiving IEP services, the public school district is required to provide services until age 21.
  • A 504 plan (Section 504: a US federal statute that prohibits discrimination based on disability) can be considered for those who require accommodations or modifications such as front-of-class seating, assistive technology devices, classroom scribes, extra time between classes, modified assignments, and enlarged text.
  • Developmental Disabilities Administration (DDA) enrollment is recommended. DDA is a US public agency that provides services and support to qualified individuals. Eligibility differs by state but is typically determined by diagnosis and/or associated cognitive/adaptive disabilities.
  • Families with limited income and resources may also qualify for supplemental security income (SSI) for their child with a disability.

Surveillance

Table 6.

Recommended Surveillance for Individuals with Familial Dysautonomia

System/ConcernEvaluationFrequency
Constitutional Assess height & weight, head circumference.Routinely in growing children
Neurogenic
dysphagia 		Assess weight, nutrition, safety of oral feeding.
  • In growing children: routinely
  • In adults: when respiratory function ↓s or respiratory infections ↑
DD / Educational
issues 		Assess developmental/educational progress.At least annually
Behavior Evaluate mental status.Routinely during interim visits
Respiratory Pulmonary function tests:
  • Spirometry before & after bronchodilator challenge to diagnose reversible obstructive disease
  • Quantitative measure of MIP & MEP to document disease progression & inform mgmt
Annually in all capable persons regardless of respiratory status; more frequently in those w/significant respiratory involvement
Sleep-disordered
breathing 		Full laboratory polysomnography incl end-tidal CO2 measurements
  • Annually regardless of previous normal studies
  • Before & 6-8 weeks after starting growth hormone therapy
Dysautonomic
crises 		Frequency & severity of hyperadrenergic crisesAnnually
Bradyarrhythmia 24-48-hr Holter monitoring regardless of previous normal studies
Orthostatic
hypotension 		Eval of symptoms & orthostatic challenge testsPerform during interim visits.
Blood pressure Monitor BP to assure optimal mgmt of BP lability to help limit neurologic progression w/age (which can be assoc w/compromised cerebral perfusion)Annual 24-hr BP monitoring
Kidney Assess kidney function to assure early detection of renal disease
  • Persons w/normal kidney function: annually
  • Persons w/CKD: per treating nephrologist
Monitor existing kidney disease.Per treating physician
Ophthalmologic Monitor eye movements, visual acuity, strabismus, corneal issues.Per treating ophthalmologist
Optic coherence tomographyRepeat annually due to accelerated & significant loss of RNFL & GCIPL.
Low vision needsPer treating low vision clinic
Sensory ataxia OT/PT assessment re activities of daily living, durable equipment needs, safety of the home/living environmentAt each visit
Musculoskeletal Spine examAnnually during growth period; less frequently thereafter
Dental Dental cleaningBiannually
General dental exam for evidence of occult biting (e.g., of buccal mucosa, tongue) & possible need for preventive dental extractionAnnually
Orthodontists & maxillofacial professionals re abnormal bite & dental crowdingPer treating dental professionals
Family support
& resources 		Assessment of caregiver needs (e.g., respite care, home nursing, coordination of multiple subspecialty appointments, equipment, medications, & supplies)At each visit

BP = blood pressure; GCIPL = ganglion cell and inner plexiform layer; MEP = maximal expiratory pressure; MIP = maximal inspiratory pressure; OT = occupational therapist; PT = physical therapist; RNFL = retinal nerve fiber layer

Agents/Circumstances to Avoid

Symptoms tend to be worse in hot or humid weather; affected individuals should try to avoid being outdoors in such conditions as much as possible.

Other situations that can exacerbate disease manifestations include a full bladder; frequent visits to the lavatory are recommended [Axelrod & Gold-von Simson 2007].

Since long car rides, coming out of a movie theater, or fatigue can also worsen symptoms, such situations should be avoided as much as possible [Axelrod & Gold-von Simson 2007].

Episodic hypertension can occur in response to emotional stress or visceral pain, and therefore should be avoided when possible [Axelrod & Gold-von Simson 2007].

Environmental situations associated with hypobaric hypoxia (e.g., aircraft flight or ascent to high altitude) pose a potential risk to individuals with daytime hypercapnia [Palma et al 2014].

Evaluation of Relatives at Risk

See Genetic Counseling for issues related to testing of at-risk relatives for genetic counseling purposes.

Pregnancy Management

Pregnancies in women with FD are considered high risk because of abrupt changes in blood pressure.

High blood pressure secondary to FD is difficult to differentiate from toxemia or other causes of pregnancy-related high blood pressure.

Awareness of volume loss and low blood pressure is important because of the absence of reflex tachycardia to low blood pressure.

Visceral pain related to contractions during labor is perceived normally; therefore, analgesia should be provided. Epidural anesthesia is preferable due to blood pressure lability during general anesthesia or spinal block [Maayan et al 2000].

Therapies Under Investigation

Search ClinicalTrials.gov in the US and EU Clinical Trials Register in Europe for access to information on clinical studies for a wide range of diseases and conditions. Note: There may not be clinical trials for this disorder.

Genetic Counseling

Genetic counseling is the process of providing individuals and families with information on the nature, mode(s) of inheritance, and implications of genetic disorders to help them make informed medical and personal decisions. The following section deals with genetic risk assessment and the use of family history and genetic testing to clarify genetic status for family members; it is not meant to address all personal, cultural, or ethical issues that may arise or to substitute for consultation with a genetics professional. —ED.

Mode of Inheritance

Familial dysautonomia (FD) is inherited in an autosomal recessive manner.

Risk to Family Members

Parents of a proband

  • The parents of an affected child are obligate heterozygotes (i.e., presumed to be carriers of one ELP1 [IKBKAP] pathogenic variant based on family history).
  • Molecular genetic testing is recommended for the parents of a proband to confirm that both parents are heterozygous for an ELP1 pathogenic variant and to allow reliable recurrence risk assessment. If a pathogenic variant is detected in only one parent and parental identity testing has confirmed biological maternity and paternity, the following possibilities should be considered:
  • Heterozygotes are asymptomatic and are not at risk of developing the disorder.

Sibs of a proband

  • If both parents are known to be heterozygous for an ELP1 pathogenic variant, each sib of an affected individual has at conception a 25% chance of being affected, a 50% chance of being an asymptomatic carrier, and a 25% chance of being unaffected and not a carrier.
  • Heterozygotes (carriers) are asymptomatic and are not at risk of developing the disorder.

Offspring of a proband

  • All offspring of an individual with FD inherit a pathogenic variant in ELP1 from their affected parent.
  • The risk that the Ashkenazi Jewish reproductive partner of an individual with FD is heterozygous for an ELP1 disease-causing allele is 1:32 (see Prevalence). Thus, the risk to the offspring of an affected individual and an Ashkenazi Jewish partner of having FD is approximately 1.5%. (The risk that a person of non-Ashkenazi Jewish ancestry is a carrier of FD is <1:150. For offspring of an individual with FD and a non-Ashkenazi Jewish reproductive partner, the risk of having FD is <1:300.)
  • It is appropriate to offer molecular genetic testing of ELP1 to the reproductive partner of an individual with FD (see Related Genetic Counseling Issues, Population screening).

Other family members. Each sib of the proband's parents is at a 50% risk of being a carrier of an ELP1 pathogenic variant.

Carrier Detection

Carrier testing for at-risk relatives requires prior identification of the ELP1 pathogenic variants in the family.

See Related Genetic Counseling Issues, Population screening for information about carrier testing in individuals who do not have a family history of FD.

Related Genetic Counseling Issues

Population screening

  • Because of the increased carrier rate for FD in individuals of Ashkenazi Jewish heritage (see Prevalence), the American College of Obstetricians and Gynecologists recommends offering carrier screening for FD to individuals of Jewish descent [ACOG 2017] (full text). Targeted analysis for pathogenic variants in ELP1 is often included in panels of "Ashkenazi Jewish pathogenic variants" offered to individuals interested in preconception or prenatal risk assessment modification.
  • If an individual has FD or is known to be a carrier of an ELP1 pathogenic variant, it is appropriate to offer molecular genetic testing of ELP1 to the individual's reproductive partner regardless of the reproductive partner’s heritage.

Family planning

  • The optimal time for determination of genetic risk and discussion of the availability of prenatal/preimplantation genetic testing is before pregnancy.
  • It is appropriate to offer genetic counseling (including discussion of potential risks to offspring and reproductive options) to young adults who are affected, are carriers, or are at risk of being carriers.

Prenatal Testing and Preimplantation Genetic Testing

Once the ELP1 pathogenic variants have been identified in an affected family member, prenatal testing for a pregnancy at increased risk and preimplantation genetic testing for FD are possible.

Differences in perspective may exist among medical professionals and within families regarding the use of prenatal testing. While most centers would consider use of prenatal testing to be a personal decision, discussion of these issues may be helpful.

Resources

GeneReviews staff has selected the following disease-specific and/or umbrella support organizations and/or registries for the benefit of individuals with this disorder and their families. GeneReviews is not responsible for the information provided by other organizations. For information on selection criteria, click here.

Molecular Genetics

Information in the Molecular Genetics and OMIM tables may differ from that elsewhere in the GeneReview: tables may contain more recent information. —ED.

Table A.

Familial Dysautonomia: Genes and Databases

GeneChromosome LocusProteinLocus-Specific DatabasesHGMDClinVar
ELP1 9q31​.3 Elongator complex protein 1 IKBKAP homepage - Leiden Muscular Dystrophy pages ELP1 ELP1

Data are compiled from the following standard references: gene from HGNC; chromosome locus from OMIM; protein from UniProt. For a description of databases (Locus Specific, HGMD, ClinVar) to which links are provided, click here.

Table B.

OMIM Entries for Familial Dysautonomia (View All in OMIM)

223900NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3
603722ELONGATOR COMPLEX PROTEIN 1; ELP1

Molecular Pathogenesis

ELP1 protein is one of the six subunits of the Elongator complex, which facilitates transcriptional elongation, and is required for efficient translation of proteins. During embryogenesis, ELP1 is expressed first in the central and peripheral nervous systems and in the gastrointestinal tract. It is then expressed in secretory tissues and cartilage, and finally in muscle. Once the organs are formed, ELP1 expression appears in the skin and mucosal tissue. Overall, expression is more prominent in the nervous system and retina, and to a lesser extent in other organs. The complete absence of ELP1 leads to embryonic lethality with failure of vasculogenesis and neurulation [Norcliffe-Kaufmann et al 2017]. Individuals with biallelic ELP1 pathogenic variants have at birth multiple lesions affecting mostly sensory (afferent) nerve fibers.

Mechanism of disease causation. The c.2204+6T>C founder variant affects the intronic splice donor site in ELP1 exon 20. The skipping of exon 20 leads to a frameshift and generation of a premature termination codon in exon 21 of ELP1 mRNA. The aberrant skipping of exon 20 is tissue specific, mostly in neurons.

ELP1-specific laboratory technical considerations. Information on two other rare variants that have not yet been published is available in the NYU Center for Dysautonomia's 2020-2021 Year in Review (pdf).

Table 7.

Notable ELP1 Pathogenic Variants

Reference SequencesDNA Nucleotide Change
(Alias 1)		Predicted Protein ChangeComment [Reference]
NM_003640​.5
NP_003631​.2 		c.2087G>Cp.Arg696ProA rare variant identified in Ashkenazi Jews [Dong et al 2002]
NM_003640​.5 c.2204+6T>C
(IVS20+6T>C)		--Founder variant that accounts for >99.5% of pathogenic variants in Ashkenazi Jews [Dong et al 2002]

Variants listed in the table have been provided by the author. GeneReviews staff have not independently verified the classification of variants.

GeneReviews follows the standard naming conventions of the Human Genome Variation Society (varnomen​.hgvs.org). See Quick Reference for an explanation of nomenclature.

1.

Variant designation that does not conform to current naming conventions

Chapter Notes

Acknowledgments

I would like to thank my supervisor, Professor Ori Efrati, Head of the Pediatric Pulmonary Unit at Sheba Medical Center, for establishing the National Center for Familial Dysautonomia as a part of our unit.

I would also like to thank Professor Horacio Kaufmann, Head of the Dysautonomia Center, New York University School of Medicine, for his support and guidance during my training at the Dysautonomia Center.

Author History

Bat-El Bar-Aluma, MD (2021-present)
Gabrielle J Halpern, MB, ChB; Beilinson Hospital, Petah Tikva (1999-2014)
Mordechai Shohat, MD; Sheba Medical Center at Tel HaShomer (1999-2021)
Monika Weisz Hubshman, MD, PhD; Rabin Medical Center, Beilinson Hospital (2014-2021)

Revision History

  • 4 November 2021 (bp) Comprehensive update posted live
  • 18 December 2014 (me) Comprehensive update posted live
  • 1 June 2010 (me) Comprehensive update posted live
  • 22 October 2007 (me) Comprehensive update posted live
  • 10 January 2005 (me) Comprehensive update posted live
  • 21 January 2003 (me) Review posted live
  • 6 November 1999 (bp) Original submission

References

Literature Cited

  • ACOG. American College of Obstetricians and Gynecologists Committee Opinion - Carrier Screening for Genetic Conditions (2017), Committee Opinion Number 691. Available online. 2017. Accessed 9-27-22.
  • Axelrod FB. Familial dysautonomia. In: Robertson D, Low PA, Polinsky RJ, eds. Primer on the Autonomic Nervous System. San Diego, CA: Academic Press; 1996:242-9.
  • Axelrod FB, Goldberg JD, Ye XY, Maayan C. Survival in familial dysautonomia: Impact of early intervention. J Pediatr. 2002;141:518–23. [PubMed: 12378191]
  • Axelrod FB, Gold-von Simson G. Hereditary sensory and autonomic neuropathies: types II, III, and IV. Orphanet J Rare Dis. 2007;2:39. [PMC free article: PMC2098750] [PubMed: 17915006]
  • Axelrod FB, Pearson J. Congenital sensory neuropathies: diagnostic distinction from familial dysautonomia. American Journal of Diseases of Children. 1984;138:947–54. [PubMed: 6206717]
  • Bernardi L, Hilz M, Stemper B, Passino C, Welsch G, Axelrod FB. Respiratory and cerebrovascular responses to hypoxia and hypercapnia in familial dysautonomia. Am J Respir Crit Care Med. 2003;167:141–9. [PubMed: 12406829]
  • Blumenfeld A, Slaugenhaupt SA, Liebert CB, Temper V, Maayan C, Gill S, Lucente DE, Idelson M, MacCormack K, Monahan MA, Mull J, Leyne M, Mendillo M, Schiripo T, Mishori E, Breakefield X, Axelrod FB, Gusella JF. Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31. Am J Hum Genet. 1999;64:1110–8. [PMC free article: PMC1377835] [PubMed: 10090896]
  • Brown CM, Stemper B, Welsch G, Brys M, Axelrod FB, Hilz MJ. Orthostatic challenge reveals impaired vascular resistance control, but normal venous pooling and capillary filtration in familial dysautonomia. Clin Sci (Lond). 2003;104:163–9. [PubMed: 12546638]
  • Di Rocco M, Stella G, Bruno C, Doria Lamba L, Bado M, Superti-Furga A. Long-term survival in Stuve-Wiedemann syndrome: a neuro-myo-skeletal disorder with manifestations of dysautonomia. Am J Med Genet A. 2003;118A:362–8. [PubMed: 12687669]
  • Dillon RC, Palma JA, Spalink CL, Altshuler D, Norcliffe-Kaufmann L, Fridman D, Papadopoulos J, Kaufmann H. Dexmedetomidine for refractory adrenergic crisis in familial dysautonomia. Clin Auton Res. 2017;27:7–15. [PMC free article: PMC5292083] [PubMed: 27752785]
  • Dong J, Edelmann L, Bajwa AM, Kornreich R, Desnick RJ. Familial dysautonomia: detection of the IKBKAP IVS20+6T --> C and R696P mutations and frequencies among Ashkenazi Jews. Am J Med Genet. 2002;110:253–7. [PubMed: 12116234]
  • Edvardson S, Cinnamon Y, Jalas C, Shaag A, Maayan C, Axelrod FB, Elpeleg O. Hereditary sensory autonomic neuropathy caused by a mutation in dystonin. Ann Neurol. 2012;71:569–72. [PubMed: 22522446]
  • Elkayam L, Matalon A, Tseng CH, Axelrod F. Prevalence and severity of renal disease in familial dysautonomia. Am J Kidney Dis. 2006;48:780–6. [PubMed: 17059997]
  • Fischer D, Schabhüttl M, Wieland T, Windhager R, Strom TM, Auer-Grumbach M. A novel missense mutation confirms ATL3 as a genefor hereditary sensory neuropathy type 1. Brain. 2014;137:e286. [PubMed: 24736309]
  • Jónsson H, Sulem P, Kehr B, Kristmundsdottir S, Zink F, Hjartarson E, Hardarson MT, Hjorleifsson KE, Eggertsson HP, Gudjonsson SA, Ward LD, Arnadottir GA, Helgason EA, Helgason H, Gylfason A, Jonasdottir A, Jonasdottir A, Rafnar T, Frigge M, Stacey SN, Th Magnusson O, Thorsteinsdottir U, Masson G, Kong A, Halldorsson BV, Helgason A, Gudbjartsson DF, Stefansson K. Parental influence on human germline de novo mutations in 1,548 trios from Iceland. Nature. 2017;549:519–22. [PubMed: 28959963]
  • Kamboj MK, Axelrod FB, David R, Geffner ME, Novogroder M, Oberfield SE, Turco JH, Maayan C, Kohn B. Growth hormone treatment in children with familial dysautonomia. J Pediatr. 2004;144:63–7. [PubMed: 14722520]
  • Kazachkov M, Palma JA, Norcliffe-Kaufmann L, Bar-Aluma BE, Spalink CL, Barnes EP, Amoroso NE, Balou SM, Bess S, Chopra A, Condos R, Efrati O, Fitzgerald K, Fridman D, Goldenberg RM, Goldhaber A, Kaufman DA, Kothare SV, Levine J, Levy J, Lubinsky AS, Maayan C, Moy LC, Rivera PJ, Rodriguez AJ, Sokol G, Sloane MF, Tan T, Kaufmann H. Respiratory care in familial dysautonomia: systematic review and expert consensus recommendations. Respir Med. 2018;141:37–46. [PMC free article: PMC6084453] [PubMed: 30053970]
  • Kfir J, Wu M, Liu M, Raju L, Schuman JS, Ishikawa H, Vanegas IM, Mendoza-Santiesteban CE, Palma JA, Norcliffe-Kaufmann L, Morgenstein B, Kaufmann H, Wollstein G. Longitudinal changes in the macula and optic nerve in familial dysautonomia. J Neurol. 2021;268:1402–9. [PMC free article: PMC7990688] [PubMed: 33180192]
  • Kornak U, Mademan I, Schinke M, Voigt M, Krawitz P, Hecht J, Barvencik F, Schinke T, Gießelmann S, Beil FT, Pou-Serradell A, Vílchez JJ, Beetz C, Deconinck T, Timmerman V, Kaether C, De Jonghe P, Hübner CA, Gal A, Amling M, Mundlos S, Baets J, Kurth I. Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3. Brain. 2014;137:683–92. [PubMed: 24459106]
  • Lehavi O, Aizenstein O, Bercovich D, Pavzner D, Shomrat R, Orr-Urtreger A, Yaron Y. Screening for familial dysautonomia in Israel: evidence for higher carrier rate among Polish Ashkenazi Jews. Genet Test. 2003;7:139–42. [PubMed: 12885336]
  • Leyne M, Mull J, Gill SP, Cuajungco MP, Oddoux C, Blumenfeld A, Maayan C, Gusella JF, Axelrod FB, Slaugenhaupt SA. Identification of the first non-Jewish mutation in familial dysautonomia. Am J Med Genet A. 2003;118A:305–8. [PubMed: 12687659]
  • Maayan C, Sela O, Axelrod F, Kidron D, Hochner-Celnikier D. Gynecological aspects of female familial dysautonomia. Isr Med Assoc J. 2000;2:679–83. [PubMed: 11062768]
  • Macefield VG, Norcliffe-Kaufmann L, Gutiérrez J, Axelrod FB, Kaufmann H. Can loss of muscle spindle afferents explain the ataxic gait in Riley-Day syndrome? Brain. 2011;134:3198–208. [PMC free article: PMC3212710] [PubMed: 22075519]
  • Mass E. Harefuah. 2016;155:490–4. [Oro-dento-facial manifestations in patients with familial dysautonomia] [PubMed: 28530322]
  • Mendoza-Santiesteban CE, Hedges Iii TR, Norcliffe-Kaufmann L, Axelrod F, Kaufmann H. Selective retinal ganglion cell loss in familial dysautonomia. J Neurol. 2014;261:702–9. [PubMed: 24487827]
  • Norcliffe-Kaufmann L, Axelrod FB, Kaufmann H. Developmental abnormalities, blood pressure variability and renal disease in Riley Day syndrome. J Hum Hypertens. 2013a;27:51–5. [PMC free article: PMC3318957] [PubMed: 22129610]
  • Norcliffe-Kaufmann L, Martinez J, Axelrod F, Kaufmann H. Hyperdopaminergic crises in familial dysautonomia: a randomized trial of carbidopa. Neurology. 2013b;80:1611–7. [PMC free article: PMC3662326] [PubMed: 23553478]
  • Norcliffe-Kaufmann L, Palma JA, Martinez J, Kaufmann H. Carbidopa for afferent baroreflex failure in familial dysautonomia: a double-blind randomized crossover clinical trial. Hypertension. 2020;76:724–31. [PMC free article: PMC7429244] [PubMed: 32654554]
  • Norcliffe-Kaufmann L, Slaugenhaupt SA, Kaufmann H. Familial dysautonomia: history, genotype, phenotype and translational research. Prog Neurobiol. 2017;152:131–48. [PubMed: 27317387]
  • Palma JA, Gileles-Hillel A, Norcliffe-Kaufmann L, Kaufmann H. Chemoreflex failure and sleep-disordered breathing in familial dysautonomia: Implications for sudden death during sleep. Auton Neurosci. 2019;218:10–15. [PMC free article: PMC6428199] [PubMed: 30890343]
  • Palma JA, Norcliffe-Kaufmann L, Fuente-Mora C, Percival L, Mendoza-Santiesteban C, Kaufmann H. Current treatments in familial dysautonomia. Expert Opin Pharmacother. 2014;15:2653–71. [PMC free article: PMC4236240] [PubMed: 25323828]
  • Palma JA, Norcliffe-Kaufmann L, Perez MA, Spalink CL, Kaufmann H. Sudden unexpected death during sleep in familial dysautonomia: a case-control study. Sleep. 2017;40:zsx083. [PMC free article: PMC5806542] [PubMed: 28521050]
  • Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 2015;17:405–24. [PMC free article: PMC4544753] [PubMed: 25741868]
  • Saini J, Axelrod FB, Maayan C, Stringer J, Smilen SW. Urinary incontinence in familial dysautonomia. Int Urogynecol J Pelvic Floor Dysfunct. 2003;14:209–13. [PubMed: 12955345]
  • Sands SA, Giarraffa P, Jacobson CM, Axelrod FB. Familial dysautonomia's impact on quality of life in childhood, adolescence, and adulthood. Acta Paediatr. 2006;95:457–62. [PubMed: 16720494]
  • Slaugenhaupt SA, Blumenfeld A, Gill SP, Leyne M, Mull J, Cuajungco MP, Liebert CB, Chadwick B, Idelson M, Reznik L, Robbins C, Makalowska I, Brownstein M, Krappmann D, Scheidereit C, Maayan C, Axelrod FB, Gusella JF. Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia. Am J Hum Genet. 2001;68:598–605. [PMC free article: PMC1274473] [PubMed: 11179008]
  • Spalink CL, Barnes E, Palma JA, Norcliffe-Kaufmann L, Kaufmann H. Intranasal dexmedetomidine for adrenergic crisis in familial dysautonomia. Clin Auton Res. 2017;27:279–82. [PMC free article: PMC5555081] [PubMed: 28674865]
  • Stenson PD, Mort M, Ball EV, Chapman M, Evans K, Azevedo L, Hayden M, Heywood S, Millar DS, Phillips AD, Cooper DN. The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting. Hum Genet. 2020;139:1197–207. [PMC free article: PMC7497289] [PubMed: 32596782]
  • Verhoeven K, De Jonghe P, Coen K, Verpoorten N, Auer-Grumbach M, Kwon JM, FitzPatrick D, Schmedding E, De Vriendt E, Jacobs A, Van Gerwen V, Wagner K, Hartung HP, Timmerman V. Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy. Am J Hum Genet. 2003;72:722–7. [PMC free article: PMC1180247] [PubMed: 12545426]
  • Welton W, Clayson D, Axelrod FB, Levine DB. Intellectual development and familial dysautonomia. Pediatrics. 1979;63:708–12. [PubMed: 440890]
Copyright © 1993-2024, University of Washington, Seattle. GeneReviews is a registered trademark of the University of Washington, Seattle. All rights reserved.

GeneReviews® chapters are owned by the University of Washington. Permission is hereby granted to reproduce, distribute, and translate copies of content materials for noncommercial research purposes only, provided that (i) credit for source (http://www.genereviews.org/) and copyright (© 1993-2024 University of Washington) are included with each copy; (ii) a link to the original material is provided whenever the material is published elsewhere on the Web; and (iii) reproducers, distributors, and/or translators comply with the GeneReviews® Copyright Notice and Usage Disclaimer. No further modifications are allowed. For clarity, excerpts of GeneReviews chapters for use in lab reports and clinic notes are a permitted use.

For more information, see the GeneReviews® Copyright Notice and Usage Disclaimer.

For questions regarding permissions or whether a specified use is allowed, contact: ude.wu@tssamda.

Bookshelf ID: NBK1180PMID: 20301359
GeneReviews by Title

Views

In this GeneReview

Bulk Download

GeneReviews Links

Tests in GTR by Gene

Related information

  • MedGen
    Related information in MedGen
  • OMIM
    Related OMIM records
  • PMC
    PubMed Central citations
  • PubMed
    Links to PubMed
  • Gene
    Locus Links

Similar articles in PubMed

See reviews...See all...

Recent Activity

ClearTurn OffTurn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...