Krabbe Disease
Synonyms: Galactocerebrosidase Deficiency, GALC Deficiency, Globoid Cell Leukodystrophy
Joseph J Orsini, PhD, Maria L Escolar, MD, MS, Melissa P Wasserstein, MD, and Michele Caggana, ScD.
Author Information and AffiliationsInitial Posting: June 19, 2000; Last Update: October 11, 2018.
Estimated reading time: 30 minutes
Summary
Clinical characteristics.
Krabbe disease comprises a spectrum ranging from infantile-onset disease (i.e., onset of extreme irritability, spasticity, and developmental delay before age 12 months) to later-onset disease (i.e., onset of manifestations after age 12 months and as late as the seventh decade). Although historically 85%-90% of symptomatic individuals with Krabbe disease diagnosed by enzyme activity alone have infantile-onset Krabbe disease and 10%-15% have later-onset Krabbe disease, the experience with newborn screening (NBS) suggests that the proportion of individuals with possible later-onset Krabbe disease is higher than previously thought. Infantile-onset Krabbe disease is characterized by normal development in the first few months followed by rapid severe neurologic deterioration; the average age of death is 24 months (range 8 months to 9 years). Later-onset Krabbe disease is much more variable in its presentation and disease course.
Diagnosis/testing.
The two diagnostic scenarios are the following:
Scenario 1. The diagnosis of Krabbe disease, suspected in a symptomatic
proband based on clinical findings (by age) and other supportive laboratory, neuroimaging, and electrophysiologic findings, is established by detection of deficient GALC enzyme activity in leukocytes. Abnormal results require follow-up
molecular genetic testing of
GALC; elevated psychosine levels can also help establish the diagnosis.
Scenario 2. In an asymptomatic newborn with low GALC enzyme activity on dried blood spot specimens on NBS urgent time-critical measurement of blood psychosine levels and
GALC molecular genetic testing is necessary to identify – before age 14 days – those newborns with evidence of infantile-onset Krabbe disease who are candidates for early treatment with hematopoietic stem cell transplantation (HSCT).
Management.
Treatment of manifestations: Treatment of a child who is symptomatic before age six months is supportive and focused on increasing the quality of life and avoiding complications. For older individuals, treatment with HSCT is individualized based on disease burden and manifestations.
Prevention of primary manifestations: Consensus guidelines recommend that asymptomatic newborns identified by either prenatal/neonatal evaluation because of a positive family history of Krabbe disease or an abnormal NBS result undergo additional testing to identify those with infantile-onset Krabbe disease. Those with laboratory findings consistent with infantile-onset Krabbe disease are candidates for HSCT before age 30 days.
Surveillance: Monitor symptomatic individuals with Krabbe disease for development of: hydrocephalus, swallowing difficulties and chronic microaspiration, scoliosis, hip subluxation, and osteopenia, decreased vision, and corneal ulcerations.
Agents/circumstances to avoid: Atypical antipsychotics and multiple medications for seizures can cause over-sedation (affecting cognition, respiratory drive, and rate of neurologic decline). Routine childhood vaccinations can accelerate disease progression.
Evaluation of relatives at risk: Couples who have had one child with molecularly confirmed infantile-onset Krabbe disease may choose prenatal molecular genetic testing in subsequent pregnancies so that newborns with biallelic GALC pathogenic variants can be promptly tested and – if appropriate -- referred for HSCT.
Genetic counseling.
Krabbe disease is inherited in an autosomal recessive manner. At conception, each sib of an affected individual has 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 GALC 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 diagnosis are possible.
Diagnosis
Krabbe disease (also known as galactocerebrosidase [GALC] deficiency) has two major phenotypes that constitute a continuum:
Infantile-onset Krabbe disease (onset <12 months), characterized by progressive neurologic deterioration in infancy and death before age two years (85%-90% of affected individuals)
Later-onset Krabbe disease (onset >12 months), with slower disease progression (10%-15%)
Suggestive Findings
The two different scenarios in which Krabbe disease could be suspected in a proband:
Scenario 1
Krabbe disease should be suspected in a symptomatic proband based on clinical findings (by age) and other supportive laboratory, neuroimaging, and electrophysiologic findings.
Clinical findings
Age <12 months (infantile-onset Krabbe disease)
Excessive crying to extreme irritability
Feeding difficulties, gastroesophageal reflux disease
Spasticity of lower extremities and fisting, with axial hypotonia
Loss of acquired milestones (smiling, cooing, and head control)
Staring episodes
Peripheral neuropathy
Age >12 months (later-onset Krabbe disease)
Slow development of motor milestones or loss of milestones (e.g., sitting without support, walking), slurred speech
Spasticity of extremities with truncal hypotonia
Vision loss, esotropia
Seizures
Peripheral neuropathy
Other supportive findings
Increased cerebrospinal fluid (CSF) protein concentration. Ranges vary by age and laboratory, normal infant range reported at 48-72 mg/dL [
Shah et al 2011]. Adult range: 18-58 mg/dL.
Note: CSF protein concentration is already increased in Stage I infantile-onset Krabbe disease (see
Clinical Description).
MRI (infantile-onset Krabbe disease) observed within the first few months of age
Abnormal brain MRI, consistent with demyelination. T
2-weighted images show involvement of periventricular white matter, deep gray matter, and centrum semiovale as well as enhancement of cranial nerves.
Subcortical U-fibers may be spared until late in the disease course [
Gupta et al 2014].
Abnormal spine MRI (enhancement of spinal nerve roots)
Abnormal electrophysiologic studies (nerve conduction velocity, brain stem auditory evoked response, visual evoked potentials)
Scenario 2
Krabbe disease should be suspected in an asymptomatic newborn with a positive result on NBS.
Currently, seven states (Illinois, Kentucky, Missouri, New York, Ohio, Pennsylvania, and Tennessee) perform NBS for GALC deficiency using dried blood spots. While the approaches to testing and cut-off values indicating a positive newborn screen vary by state, all results suggesting GALC deficiency require immediate follow-up studies (see Establishing the Diagnosis, Scenario 2).
Establishing the Diagnosis
Scenario 1
The testing required to establish the diagnosis Krabbe disease in a symptomatic proband. In individuals with some or all of the suggestive findings of infantile-onset Krabbe disease or later-onset Krabbe disease, the diagnosis is established by detection of deficient GALC enzyme activity in leukocytes. Abnormal results require follow-up molecular genetic testing of GALC. For children with infantile-onset Krabbe disease, elevated psychosine levels in dried blood spot specimens confirm the diagnosis; however, in individuals who have later-onset Krabbe disease or have progressed to the later stages of the infantile form of disease, it is not yet known if psychosine concentrations are consistently elevated.
Galactocerebrosidase
(GALC) enzyme activity is measured in leukocytes isolated from whole heparinized blood or cultured skin fibroblasts. The substrate used (i.e., radiometric substrate, fluorescent substrate, or mass spectrometry substrate) depends on the laboratory.
Very low GALC enzyme activity (0%-5% of normal activityl) is observed in all individuals with Krabbe disease who are symptomatic. Note: Low GALC activity can result from pseudodeficiency alleles (benign
GALC variants that reduce enzyme activity in vitro but do not cause disease),
carrier status for a
GALC pathogenic variant, or saposin A deficiency (see
Molecular Genetics).
If GALC enzyme activity in leukocytes is completely normal, no additional biochemical testing is required to exclude Krabbe disease. However, if psychosine was elevated in such cases, a diagnosis of saposin A deficiency should be considered.
Psychosine concentration
Infantile-onset Krabbe disease. Very elevated concentrations of psychosine (usually >10 nmol/L) are strongly supportive of early symptomatic Krabbe disease [
Turgeon et al 2015,
Escolar et al 2017,
Minter Baerg et al 2018]. Note that psychosine concentrations may drop significantly in the later stages of infantile-onset Krabbe disease and that psychosine may also be elevated in individuals with saposin A deficiency.
Later-onset Krabbe disease. Psychosine concentrations may not be markedly elevated and may depend on how long the patient has been symptomatic [
Escolar et al 2017].
Molecular testing involves single-gene testing. Sequence analysis of GALC and targeted analysis for the common GALC 30-kilobase deletion (30kb del) is performed [Luzi et al 1995, Rafi et al 1995]. Gene-targeted deletion/duplication analysis should also be performed, at least when the suspicion of Krabbe disease is high and only one GALC pathogenic variant has been detected by sequence analysis. See Table 1.
Table 1.
Molecular Genetic Testing Used in Krabbe Disease (Galactosylcerebrosidase Deficiency)
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| Gene 1 | Method | Proportion of Probands with Pathogenic Variants 2 Detectable by Method |
|---|
|
GALC
| Sequence analysis 3 | 55%-65% 4 |
| Targeted analysis for 30kb del | 35%-45% 5 |
| Gene-targeted deletion/duplication analysis 6 | See footnote 7. |
- 1.
- 2.
- 3.
- 4.
- 5.
This large deletion accounts for approximately 35% of the pathogenic variants in individuals with Krabbe disease of Mexican heritage [D.Wenger, personal experience] and 45% of the pathogenic variants in individuals with Krabbe disease of European ancestry [Luzi et al 1995, Rafi et al 1995].
- 6.
Gene-targeted deletion/duplication analysis detects intragenic deletions or duplications. Methods used may include a range of techniques such as quantitative PCR, long-range PCR, multiplex ligation-dependent probe amplification (MLPA), and a gene-targeted microarray designed to detect single exon deletions or duplications.
- 7.
Scenario 2
The testing required to establish the diagnosis Krabbe disease in an asymptomatic infant identified on NBS. Presumptive positive newborn screening results for Krabbe disease must be followed up urgently with time-critical biochemical and molecular genetic studies to identify those newborns with biochemical and molecular genetic evidence of infantile-onset Krabbe disease before age 14 days who are candidates for early treatment with hematopoietic stem cell transplantation (HSCT) (see Management, Prevention of Primary Manifestations) [Wasserstein et al 2016, Kwon et al 2018].
Note that regardless of the method used to assay GALC enzyme activity, low GALC activity in dried blood spots and/or leukocytes in asymptomatic newborns is not sufficiently specific to diagnose Krabbe disease, let alone to distinguish between infantile-onset and later-onset Krabbe disease. In addition to certain environmental factors, low GALC activity can result from pseudodeficiency alleles (benign GALC variants that reduce enzyme activity in vitro but do not cause disease), heterozygosity (i.e., carrier state) for one GALC pathogenic variant, and GALC variants observed in later-onset Krabbe disease.
Note: (1) The common 30-kb deletion may be tested for by allele-specific or breakpoint PCR as part of the first-tier sequencing assay [Luzi et al 1995, Rafi et al 1995]. (2) The necessary turn-around time for sequencing and deletion/duplication analysis in this scenario is shorter than routinely offered for diagnostic purposes; therefore, specific arrangements need to be made to ensure expedited testing.
Identification of biallelic GALC pathogenic variants known to be associated with infantile-onset Krabbe disease or classified as pathogenic or likely pathogenic further confirms the diagnosis of infantile-onset Krabbe disease [Orsini et al 2016].
Of note, the vast majority of infants identified through the New York State NBS program who have low GALC enzyme activity and two presumptive pathogenic GALC variants do not have signs or symptoms of infantile-onset disease [Wasserstein et al 2016] and thus are considered to be at risk for later-onset Krabbe disease. A revised definition of risk for infantile-onset Krabbe disease based on results of psychosine concentration and GALC molecular genetic testing that is under review is expected to significantly decrease the proportion of infants designated as at risk for infantile-onset Krabbe disease identified by NBS [Author, personal communication].
Clinical Characteristics
Clinical Description
Historically, 85%-90% of symptomatic individuals with Krabbe disease diagnosed by enzyme activity alone had infantile-onset Krabbe disease (i.e., onset of extreme irritability, spasticity, and developmental delay before age 12 months) and 10%-15% had later-onset Krabbe disease (i.e., onset of manifestations after age 12 months and as late as the seventh decade). In contrast, the vast majority of infants identified through the New York State newborn screening (NBS) program who have low GALC enzyme activity and two presumptive pathogenic GALC variants do not have signs or symptoms of infantile-onset disease [Wasserstein et al 2016]; thus, it is likely that the proportion of individuals with later-onset Krabbe disease is higher than previously thought [Author, personal communication].
Infantile-Onset Krabbe Disease
Infantile-onset Krabbe disease typically has four stages:
Stage I. The infant, apparently normal for the first few months after birth, begins to cry frequently without apparent cause. Many keep their hands tightly fisted. Feeding difficulties and gastroesophageal reflux may result in progressive weight loss leading to emaciation. In some infants, peripheral neuropathy is a presenting feature with no other neurologic features appreciated for several months [
Korn-Lubetzki et al 2003].
Stage II is characterized by rapid severe neurologic deterioration with decorticate posturing (marked hypertonicity with extended and crossed legs, flexed arms, and trunk hyperextension [opisthotonus]). Tendon reflexes are absent. Staring episodes and minor muscle spasms occur. Optic atrophy and sluggish pupillary reactions to light are common.
Stage III is characterized by poor control of temperature and heart rate, as well as blindness, deafness, and seizures.
Stage IV is characterized by very low muscle tone and absence of voluntary movement.
The average age of death in children with infantile-onset Krabbe disease is 24 months; however, some succumb by age eight months from infections and respiratory failure, while others live up to age nine years.
Symptoms and signs are confined to the nervous system. No visceromegaly is present. Head size may be large or small; hydrocephalus with increased intracranial pressure has been observed. Macular cherry-red spots were described in one individual.
One infant, diagnosed with GALC deficiency in utero, had normal psychomotor development for the first two months of life but lost deep tendon reflexes by age five weeks, had markedly reduced nerve conduction velocities at age seven weeks, and developed neck muscle weakness at age three months [Lieberman et al 1980]. These findings suggest that detailed examination could reveal clinical manifestations of infantile-onset Krabbe disease earlier than the reported age of onset.
Some infants with a positive NBS (and subsequently confirmed to have infantile-onset Krabbe disease) had at least one of the following in the first weeks of life: clonus in the lower extremities, difficulty feeding, abnormal nerve conduction velocity, elevated CSF protein, abnormal brain MRI.
Later-Onset Krabbe Disease
Children with onset between ages 12 months and three years can be clinically normal until they manifest gait changes, hemiplegia/diplegia, visual impairment, febrile seizures, and/or tremors. Because myelination occurs very rapidly between birth and age two years, symptoms develop more rapidly at this age than after age two years.
Children with disease onset between ages 24 months and four years can initially manifest loss of milestones and vision (including rapid loss of vision) or gait changes and seizures.
Although disease progression is variable, children who develop symptoms between ages nine months and four years may have rapid worsening of symptoms shortly after presentation. In most instances death occurs approximately four to six years after onset [M Escolar, personal communication].
Initial manifestations in children older than age six years may be behavioral difficulties (attention-deficit/hyperactivity disorder and mood disorders) followed by motor difficulty. They often decline rapidly soon after disease onset [Fiumara et al 2011].
Some individuals with onset in adolescence and adulthood present with loss of manual dexterity, burning paresthesias in their extremities, and weakness without intellectual deterioration; others become bedridden and continue to deteriorate mentally and physically [Kolodny et al 1991, Satoh et al 1997, Jardim et al 1999, Wenger 2003]. Presenting manifestations in adult-onset disease can also include unilateral upper-limb weakness and lower-limb hypoesthesia [Debs et al 2013]. Disease progression is generally slower in the adult-onset disease than in adolescent-onset disease.
The adult-onset group includes individuals in whom the diagnosis was first made in adulthood (because the subtle symptoms present earlier in life did not prompt biochemical testing) as well as individuals considered completely normal until manifestations began after age 20 years [Kolodny et al 1991, Satoh et al 1997, Wenger 2003]. An example of the former is a woman reported by Kolodny et al [1991] (case 15) who had been "shaky" in childhood, walked slowly with a stiff and wide-based gait, and had progressive, generalized neurologic deterioration after age 40 years. She died of pneumonia at age 73 years. An example of the latter is a woman who developed slowly progressive spastic paraparesis at age 38 years. Demyelination identified on MRI was confined to the corticospinal tract [Satoh et al 1997].
Peripheral neuropathy is less common in later-onset disease (affecting about half of affected individuals) than in infantile-onset disease (affecting nearly all affected individuals) [Husain et al 2004, Siddiqi et al 2006, Debs et al 2013].
Survival varies widely among persons with later-onset disease; the median age is eight years after symptom onset [Bascou et al 2018].
Neurophysiologic findings in later-onset Krabbe disease include the following:
Electroencephalogram (EEG). While normal in the initial stages, the EEG gradually becomes abnormal. Background activity becomes slow and disorganized, with changes that may be asymmetric.
Cerebrospinal fluid protein levels can vary widely but are always elevated in the infantile-onset disease.
Electrophysiologic studies. Although motor nerve conduction velocities are generally low, they are normal in some adults with an enzymatically confirmed diagnosis.
MRI. In general, brain MRI detects demyelination in the brain stem and cerebellum more clearly than CT in the early stage of later-onset Krabbe disease; however, some infants younger than age six months have a deceptively normal MRI because of the low contrast between gray and white matter in this period of brain development. Of note, scoring of atrophy of the midbrain assists in evaluating general disease progression [Zuccoli et al 2015].
Diffusion tensor imaging (DTI) of the brain. DTI is the preferred imaging modality for evaluating asymptomatic infants with Krabbe disease detected by NBS [Gupta et al 2014] (see Management, Prevention of Primary Manifestations).
Genotype-Phenotype Correlations
Infantile-onset Krabbe disease results from severe loss of galactocerebrosidase activity due to:
Homozygosity for the common
GALC 30-kb
deletion;
Later-onset Krabbe disease. The following genotypes have been observed in individuals with later-onset disease:
p.Gly286Asp + another severe
allele
The p.Gly57Ser variant, a founder variant common in Catania, Italy, is associated with late-onset Krabbe disease in both the homozygous and compound heterozygous states [Lissens et al 2007].
Note that although p.Gly286Asp has been observed in individuals with a milder phenotype, to date it is not possible to predict the clinical course in a given individual.
Nomenclature
The protein encoded by GALC is termed galactocerebrosidase in UniProt, the standard reference for GeneReviews (see Table A). Because additional terms for this protein are used in the published literature, Krabbe disease may also be referred to as:
Galactosylceramidase deficiency
Galactosylcerebrosidase deficiency
β-galactocerebrosidase deficiency
Prevalence
Krabbe disease occurs in approximately one in 250,000 births in the United States [Barczykowski et al 2012] and approximately one in 100,000 births in Europe [Wenger et al 2013]; with the median prevalence varying widely between countries [Tappino et al 2010].
A very high incidence of Krabbe disease is found in a Druze community in northern Israel and two Muslim Arab villages located near Jerusalem where the carrier rate is estimated at one in six [Rafi et al 1996].
Differential Diagnosis
Although a history of normal development for the first few months after birth followed by psychomotor deterioration differentiates Krabbe disease from non-progressive CNS disorders of congenital or perinatal origin, it is nonetheless often difficult to differentiate Krabbe disease from other degenerative diseases. Individuals of any age with progressive deterioration of the central or peripheral nervous system should be evaluated for galactocerebrosidase (GALC) deficiency.
The following disorders, ordered by mode of inheritance, should be considered in the differential diagnosis.
Autosomal Recessive
Arylsulfatase A deficiency
(metachromatic leukodystrophy, MLD) is characterized by three clinical subtypes that can closely resemble late-onset Krabbe disease:
Late-infantile MLD (50%-60% of individuals) with onset between age one and three years
Juvenile MLD (~20%-30%) with onset between age four years and sexual maturity (12-14 years)
Adult MLD (~15%-20%) with onset after sexual maturity
Biallelic pathogenic variants in ARSA are causative.
Hexosaminidase A deficiency results in a group of neurodegenerative disorders caused by the intralysosomal storage of the specific glycosphingolipid, GM2 ganglioside. Tay-Sachs disease, the prototype hexosaminidase A deficiency, is characterized by loss of motor skills beginning between ages three and six months with progressive evidence of neurodegeneration, including seizures, macular cherry-red spots, and blindness. Total incapacitation and death usually occur before age four years. The juvenile, chronic, and adult-onset variants of hexosaminidase A deficiency have later onset, slower progression, and more variable neurologic findings, including progressive dystonia, spinocerebellar degeneration, motor neuron disease, and in some individuals with adult-onset disease, a bipolar form of psychosis. Biallelic pathogenic variants in HEXA are causative.
Canavan disease. Neonatal/infantile (severe) Canavan disease is characterized by evidence of developmental delays by age three to five months with severe hypotonia and failure to achieve independent sitting, ambulation, or speech. Hypotonia evolves into spasticity and assistance with feeding becomes necessary. Life expectancy is usually into the second decade. Most individuals with Canavan disease have macrocephaly, which is a variable finding in individuals with Krabbe disease. MRI shows prominent involvement of subcortical white matter. Biallelic pathogenic variants in ASPA are causative.
Saposin A deficiency (OMIM 611722). An infant from a consanguineous union who demonstrated abnormal myelination resembling Krabbe disease was found to be homozygous for a pathogenic variant in the saposin A region of PSAP, which codes prosaposin, a heat-stable protein that interacts with the GALC enzyme to catalyze the hydrolysis of the natural lipid substrates [Spiegel et al 2005]. Saposin A deficiency may also be associated with reduced GALC enzyme activity and elevated psychosine concentrations. Biallelic pathogenic variants in PSAP are causative.
X-Linked
X-linked adrenoleukodystrophy
(X-ALD) affects the nervous system white matter and the adrenal cortex. The childhood cerebral form of X-ALD is in the differential diagnosis of Krabbe disease. It manifests most commonly between age four and eight years. It initially resembles attention deficit disorder; progressive impairment of cognition, behavior, vision, hearing, and motor function follow the initial symptoms and often lead to total disability within two years. A hemizygous ABCD1 pathogenic variant is causative.
Pelizaeus-Merzbacher disease (PMD) is part of the phenotypic spectrum of PLP1-related disorders of central nervous system myelin formation. The phenotypes that can be observed in males with this disorder range from PMD to spastic paraplegia 2 (SPG2); a wide range of phenotypes can be observed in members of the same family. PMD typically manifests in infancy or early childhood with nystagmus, hypotonia, and cognitive impairment and progresses to severe spasticity and ataxia. Life span is shortened. A hemizygous PLP1 pathogenic variant is causative.
Autosomal Dominant
Alexander disease is a progressive disorder of cerebral white matter that predominantly affects infants and children and has variable life expectancy. The later-onset forms present with a slower clinical course. The infantile form comprises about 42% of affected individuals, the juvenile form about 22%, and the adult form about 33%. A neonatal form is also recognized. The neonatal form leads to severe disability or death within two years. The infantile form presents in the first two years of life typically with progressive psychomotor retardation with loss of developmental milestones, megalencephaly, frontal bossing, and seizures. Affected individuals survive a few weeks to several years. The juvenile form usually presents between age four and ten years, occasionally in the mid-teens. Survival is variable, ranging from the early teens to the 20s-30s. Affected individuals can present with bulbar/pseudobulbar signs, poor coordination (ataxia), gradual loss of intellectual function, seizures, normocephaly or megalencephaly, and breathing problems. A heterozygous pathogenic variant in GFAP is causative.
Autosomal dominant leukodystrophy with dysautonomia is a slowly progressive disorder of central nervous system white matter characterized by onset of autonomic dysfunction in the fourth to fifth decade, followed in months to years by pyramidal and cerebellar involvement. Autonomic dysfunction can include bladder dysfunction, constipation, postural hypotension, feeding difficulties, erectile dysfunction, and (less often) impaired sweating. Pyramidal signs are often more prominent in the lower extremities (i.e., spastic weakness, hypertonia, clonus, brisk deep tendon reflexes, and bilateral Babinski signs). Cerebellar signs typically appear at the same time as the pyramidal signs and can include gait ataxia, dysdiadochokinesia, intention tremor, dysmetria, and nystagmus. Although cognitive function is usually preserved or only mildly impaired early in the disease course, dementia and psychiatric manifestations can occur as late manifestations. Affected individuals may survive for decades after onset. Either an LMNB1 duplication or (more rarely) a large heterozygous deletion upstream of the LMNB1 promoter is causative.
Management
Evaluations Following Initial Diagnosis
To establish the extent of disease and needs of a symptomatic individual
diagnosed with Krabbe disease (i.e., Scenario 1), the evaluations summarized in this section (if not performed as part of the evaluation that led to the diagnosis) are recommended:
Neurologic and developmental examination
Brain stem auditory evoked response to assess hearing and auditory neuropathy
Brain MRI (DTI preferred) to understand disease progression and anticipate care needs (e.g., atrophy of brain stem is likely associated with apnea and temperature instability).
Nerve conduction velocity to help understand the peripheral nerve involvement and development of muscle weakness
Visual evoked potential to help understand the best approach to visual and developmental therapy
Consultation with a clinical geneticist and/or genetic counselor
Treatment of Manifestations
Symptomatic individual. For a child younger than age six months who is in Stage II or III of infantile-onset Krabbe disease (see Clinical Description), treatment is supportive and focused on increasing the quality of life and avoiding complications (Table 2) [Escolar et al 2016].
Table 2.
Treatment of Manifestations in Individuals with Krabbe Disease Who Have NOT Undergone Hematopoietic Stem Cell Transplantation (HSCT)
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| System/Concern | Manifestation | Treatment |
|---|
|
Gastrointestinal
| Vomiting & gastroesophageal reflux disease (GERD) | Maintainence of upright positioning during & after feeding Consideration of proton pump inhibitors in those age >1 yr Nissen fundoplication w/gastrostomy tube (G-tube) placement.
|
| Dysphagia | Modifying texture & thickness of foods using commercial thickening agents can help w/swallowing difficulties. Swallowing ability may be improved by providing tiny tastes of food or juice several times per day in non-feeders. Consideration of nasogastric tube or gastric tube placement
|
| Constipation |
|
|
Neurologic
| Spasticity |
|
| Neuropathic pain; seizures | Standard anti-seizure medications; monotherapy is preferred, if possible. Gabapentin may decrease neuropathic pain & can be used for control of seizures in some.
|
|
Musculoskeletal
| Contractures |
|
|
Respiratory
| Excessive airway secretions | Chest physiotherapy Postural drainage Suctioning device
|
|
Genitourinary
| Urinary tract infections |
|
|
Eyes
| Delayed pupillary response, difficulty w/upward gaze & palpebral weakness | |
| Corneal ulcers |
|
|
Dental
| Delayed dentition | |
Older individuals with mild manifestations. Treatment (based on standard practice) is tailored to the manifestations in each individual.
Prevention of Primary Manifestations
Escolar et al [2005] reported that all 11 asymptomatic newborns (diagnosed prenatally or shortly after birth because of a family history of Krabbe disease) who underwent HSCT between ages 12 and 44 days had stable engraftment of donor hematopoietic stem cells that provided a long-term source of GALC enzyme. Follow up over four months to six years has thus far revealed that while most children had normal cognitive ability and receptive language, they eventually developed speech and motor difficulties (including spasticity).
Wasserstein et al [2016] reported outcomes for five infants from four families detected by the New York State newborn screening program. Two of the five were sibs. All but the first-born in the sib pair underwent HSCT between days 24 and 41 of life. Outcomes for the four who underwent HSCT were not ideal, likely due to disease severity at the time of the transplantation. More recently, several newborns identified through other state newborn screening programs have had more positive outcomes [Orsini, personal observation].
Wright et al [2017] reported a 15-year study of outcomes for 18 individuals presumed to have a form of infantile-onset Krabbe disease who underwent HSCT in the first seven weeks of life. Following early HSCT, the long-term outcome of motor function reflected the severity of corticospinal tract involvement at birth. Peripheral nerve disease progressed with time, causing severe muscular atrophy and scoliosis. Compared to children not treated as babies, those treated early with HSCT can live relatively normal lives with variable motor disabilities until the teen years when the disease may progress. Mortality was 25%, slightly less than general mortality for non-malignant diseases. Outcomes following HSCT vary widely: some individuals live completely normal lives, whereas others are disabled (ranging from reliance on walkers for mobility to quadriplegia). The outcomes depend on how early disease is detected, the severity of disease, and progression of the disease prior to treatment.
Asymptomatic newborns with infantile-onset Krabbe disease. Consensus guidelines recommend that asymptomatic newborns identified by either prenatal/neonatal evaluation because of a positive family history of Krabbe disease (see Evaluation of Relatives at Risk) or an abnormal newborn screening result undergo additional testing to identify those with infantile-onset Krabbe disease (see Establishing the Diagnosis, Scenario 2). Those with laboratory findings consistent with infantile-onset Krabbe disease are thus candidates for HSCT before age 14 days [Kwon et al 2018].
Asymptomatic newborns with abnormal newborn screening results presumed to be at risk for later-onset Krabbe disease. No guidelines have been published for monitoring these at-risk individuals and to date there are no validated markers that can predict later disease onset [Wasserstein et al 2016].
Symptomatic individuals with later-onset Krabbe disease. The manifestations of Krabbe disease progress more slowly; thus, individuals with later-onset Krabbe disease diagnosed early enough in the disease course may benefit from HSCT. In a single report by Laule et al [2018] treatment was found to arrest demyelination and axonal loss.
Prevention of Secondary Complications
Symptomatic individuals with Krabbe disease
Physical therapy can improve strength, mobility, flexibility, and function.
Erythromycin may be useful as a prophylactic antibiotic and may also improve gastrointestinal motility.
Surveillance
Symptomatic individuals with Krabbe disease
Monitor for development of:
Hydrocephalus and need for VP shunt
Scoliosis, hip subluxation, and osteopenia (via dual-energy x-ray absorptiometry [DXA] scan)
Decreased vision and corneal ulcerations
Swallowing difficulties and chronic microaspiration (via modified barium swallow)
Agents/Circumstances to Avoid
Symptomatic individuals with Krabbe disease
Atypical antipsychotics and multiple medications for seizures [Author, personal experience], which can: overly sedate patients, further affecting cognition; affect respiratory drive; and accelerate the neurodegenerative cascade
Routine childhood vaccinations, including live virus vaccines, as the resulting immune response may accelerate disease progression [
Escolar et al 2016]
Prolonged indwelling catheters for urinary retention due to the high risk of infection
Therapies Under Investigation
Studies are being conducted using well-characterized animal models to investigate other treatment options including enzyme replacement therapy, neural stem cell transplantation, substrate reduction therapy, and chemical chaperone therapy. To date experimental "combination therapies" (HSCT together with gene therapy) in the GALC-deficient murine model have demonstrated the potential to further advance treatment of GALC deficiency by synergistically increasing the life span of the treated mice [Reddy et al 2013, Rafi et al 2015, Ungari et al 2015].
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.
Risk to Family Members
Parents of a proband
Sibs of a proband
Offspring of a proband with later-onset Krabbe disease. The offspring of an individual with later-onset Krabbe disease are obligate heterozygotes (carriers) for a GALC pathogenic variant.
Other family members. Each sib of the proband's parents (aunts and uncles of the proband) and each grandparent is at a 50% risk of being a carrier of a GALC pathogenic variant.
Carrier Detection
At-risk family members. Carrier testing for at-risk relatives requires prior identification of the GALC pathogenic variants in the family.
Prenatal Testing and Preimplantation Genetic Testing
Molecular genetic testing. Once the GALC pathogenic variants have been identified in an affected family member, prenatal testing for a pregnancy at increased risk and preimplantation genetic testing are possible.
Biochemical genetic testing. Prenatal testing by GALC enzyme testing is not offered in the United States.
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.
National Library of Medicine Genetics Home Reference
Newborn Screening in Your State
Health Resources & Services Administration
Partners for Krabbe Research
The Legacy of Angels Foundation
PO Box 1014
Prior Lake MN 55372
Email: info@tloaf.org
United Leukodystrophy Foundation
Phone: 800-SAV-LIVE; 815-748-3211
Email: office@ulf.org
Myelin Disorders Bioregistry Project
Phone: 215-590-1719
Email: sherbinio@chop.edu
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.
Krabbe Disease: Genes and Databases
View in own window
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.
Gene structure.
GALC is approximately 57 kb in length with 17 exons that code for a 685-amino-acid precursor protein that is processed – after cleavage of the 16-amino-acid signal peptide – into a protein of 669 amino acids. Historical nomenclature numbered amino acids beginning at -16; therefore, codon numbers in older references [Wenger et al 1997] may differ from current standard nomenclature by 16 amino acids.
Benign variants. Three common GALC variants (p.Arg184Cys, p.Asp248Asn, and p.Ile562Thr) attenuate GALC enzyme activity [Saavedra-Matiz et al 2016]. Although not disease-causing, their presence complicates the interpretation of the clinical significance of low enzyme activity. However, p.Ile562Thr [legacy: p.Ile546Thr] has been shown to be disease causing when in cis with another mild pathogenic variant, e.g. p.Thr112Ala [legacy: p.Thr96Ala] [Wenger et al 2014, Saavedra-Matiz et al 2016]. Furthermore, other non-disease-causing variants reduce in vitro enzyme activity measurements detected by newborn screening in asymptomatic individuals.
Pathogenic variants. More than 200 pathogenic variants including nonsense, frameshift, splice site, and missense variants have been identified. It is often not possible to predict the clinical presentation from the location or type of variant.
The 30-kb deletion, the most common pathogenic variant, which begins within the large intron 10 and extends beyond the end of the gene, accounts for approximately 45% of pathogenic variants in persons of European ancestry. This deletion comprises a significant proportion of pathogenic variants in individuals of Mexican, Pakistani, and Indian heritage. When in the homozygous state or in the compound heterozygous state with another severe pathogenic variant this deletion results in infantile-onset Krabbe disease. Thus far, all individuals with Krabbe disease identified through newborn screening have a least one copy of the deletion.
Several other pathogenic variants associated with infantile-onset Krabbe disease (p.Thr529Met, p.Tyr567Ser, and c.1472delA) make up another 15% of the abnormal alleles in individuals of European ancestry [Kleijer et al 1997, Wenger et al 1997].
A 7.4-kb deletion has also been observed in multiple patients.
The pathogenic variant p.Gly286Asp results in the later-onset form of GALC deficiency, even when present with the 30-kb deletion as the second allele.
A founder variant common in Catania, Italy, p.Gly57Ser, is associated with later-onset Krabbe disease in both the homozygous and compound heterozygous states [Lissens et al 2007]. In general the genotypes of individuals with Krabbe disease are complex, with combinations of benign variants and pathogenic variants.
When variants of unknown significance are identified, elevated psychosine (within reference range for infantile-onset Krabbe disease) and low GALC activity are suggestive findings of infantile-onset Krabbe disease.
A more complete catalog of reported GALC variants is available in Wenger et al [2013].
Table 3.
Common GALC Polymorphisms and Pathogenic Variants
View in own window
Variant
Classification | DNA Nucleotide Change
(Alias 1) | Predicted Protein Change
(Alias 1) | Reference Sequences |
|---|
|
Benign
| c.550C>T | p.Arg184Cys
(p.Arg168Cys) |
NM_000153.3
NP_000144.2
|
| c.742G>A | p.Asp248Asn
(p.Asp232Asn) |
| c.1685T>C | p.Ile562Thr
(p.Ile546Thr) |
|
Pathogenic
| (30-kb deletion) 2 | -- |
c.169G>A
(121G>A) | p.Gly57Ser
(Gly41Ser) |
c.334A>G
(286A>G) | p.Thr112Ala
(Thr96Ala) |
c.560A>T
(512A>T) | p.Asp187Val
(Asp171Val) |
c.857G>A
(809G>A) | p.Gly286Asp 3
(Gly270Asp) |
c.953C>T
(944C>T) | p.Pro318Arg
(p.Gly302Arg) |
c.1472delA
(1424delA) | p.Lys491ArgfsTer62 |
c.1586C>T
(1538C>T) | p.Thr529Met
(Thr513Met) |
c.1700A>C
(1652A>C) | p.Tyr567Ser
(Tyr551Ser) |
c.1901T>C
(1853T>C) | p.Leu634Ser 4
(Leu618Ser) |
See Quick Reference for an explanation of nomenclature. GeneReviews follows the standard naming conventions of the Human Genome Variation Society (varnomen.hgvs.org).
- 1.
Historical variant designations that do not conform to current naming conventions. In this instance, the variant designations conform to the cDNA reference sequence in the HGMD database (see Table A) and some publications.
- 2.
Begins in intron 10 and deletes the remainder of the gene and additional contiguous sequences
- 3.
- 4.
Normal gene product. The 80-kd precursor protein contains six potential glycosylation sites and is proteolytically cut into the active 50-kd and 30-kd subunits. These subunits are not active individually, but aggregate into a very high hydrophobic molecular-weight complex.
Abnormal gene product. Loss or significant reduction of galactosylceramidase function results in Krabbe disease.
Chapter Notes
Author History
Michele Caggana, ScD (2018-present)
Stephanie Coppola, BS; Thomas Jefferson University, Pennsylvania (2004-2006)
Maria L Escolar, MD (2018-present)
Joseph J Orsini, PhD (2018-present)
Melissa P Wasserstein, MD (2018-present)
David A Wenger, PhD; Thomas Jefferson University, Pennsylvania (2000-2018)
Revision History
11 October 2018 (bp) Comprehensive update posted live
31 March 2011 (me) Comprehensive update posted live
3 January 2007 (me) Comprehensive update posted live
27 September 2004 (me) Comprehensive update posted live
25 November 2002 (me) Comprehensive update posted live
19 June 2000 (me) Review posted live
February 2000 (dw) Original submission
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