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Multiple epiphyseal dysplasia, Beighton type(EDMMD)

MedGen UID:
377049
Concept ID:
C1851536
Disease or Syndrome
Synonym: Epiphyseal dysplasia, multiple, with myopia and conductive deafness
Modes of inheritance:
Autosomal dominant inheritance
MedGen UID:
141047
Concept ID:
C0443147
Intellectual Product
Source: Orphanet
A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.
 
Gene (location): COL2A1 (12q13.11)
 
Monarch Initiative: MONDO:0007562
OMIM®: 132450
Orphanet: ORPHA166011

Definition

A rare primary bone dysplasia characterized by the association of multiple epiphyseal dysplasia, visual impairment (with early-onset progressive myopia, retinal thinning, and cataracts), and conductive hearing loss. Patients are of short stature and present brachydactyly, genu valgus deformity, and joint pain. [from ORDO]

Clinical features

From HPO
Brachydactyly
MedGen UID:
67454
Concept ID:
C0221357
Congenital Abnormality
Digits that appear disproportionately short compared to the hand/foot. The word brachydactyly is used here to describe a series distinct patterns of shortened digits (brachydactyly types A-E). This is the sense used here.
Coxa valga
MedGen UID:
116080
Concept ID:
C0239137
Finding
Coxa valga is a deformity of the hip in which the angle between the femoral shaft and the femoral neck is increased compared to age-adjusted values (about 150 degrees in newborns gradually reducing to 120-130 degrees in adults).
Genu valgum
MedGen UID:
154364
Concept ID:
C0576093
Anatomical Abnormality
The legs angle inward, such that the knees are close together and the ankles far apart.
Short phalanx of finger
MedGen UID:
163753
Concept ID:
C0877165
Finding
Short (hypoplastic) phalanx of finger, affecting one or more phalanges.
Short stature
MedGen UID:
87607
Concept ID:
C0349588
Finding
A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms).
Conductive hearing impairment
MedGen UID:
9163
Concept ID:
C0018777
Disease or Syndrome
An abnormality of vibrational conductance of sound to the inner ear leading to impairment of sensory perception of sound.
Epiphyseal dysplasia
MedGen UID:
95932
Concept ID:
C0392476
Congenital Abnormality
Narrow mouth
MedGen UID:
44435
Concept ID:
C0026034
Congenital Abnormality
Distance between the commissures of the mouth more than 2 SD below the mean. Alternatively, an apparently decreased width of the oral aperture (subjective).
Round face
MedGen UID:
116087
Concept ID:
C0239479
Finding
The facial appearance is more circular than usual as viewed from the front.
Flat face
MedGen UID:
342829
Concept ID:
C1853241
Finding
Absence of concavity or convexity of the face when viewed in profile.
Myopia
MedGen UID:
44558
Concept ID:
C0027092
Disease or Syndrome
Nearsightedness, also known as myopia, is an eye condition that causes blurry distance vision. People who are nearsighted have more trouble seeing things that are far away (such as when driving) than things that are close up (such as when reading or using a computer). If it is not treated with corrective lenses or surgery, nearsightedness can lead to squinting, eyestrain, headaches, and significant visual impairment.\n\nNearsightedness usually begins in childhood or adolescence. It tends to worsen with age until adulthood, when it may stop getting worse (stabilize). In some people, nearsightedness improves in later adulthood.\n\nFor normal vision, light passes through the clear cornea at the front of the eye and is focused by the lens onto the surface of the retina, which is the lining of the back of the eye that contains light-sensing cells. People who are nearsighted typically have eyeballs that are too long from front to back. As a result, light entering the eye is focused too far forward, in front of the retina instead of on its surface. It is this change that causes distant objects to appear blurry. The longer the eyeball is, the farther forward light rays will be focused and the more severely nearsighted a person will be.\n\nNearsightedness is measured by how powerful a lens must be to correct it. The standard unit of lens power is called a diopter. Negative (minus) powered lenses are used to correct nearsightedness. The more severe a person's nearsightedness, the larger the number of diopters required for correction. In an individual with nearsightedness, one eye may be more nearsighted than the other.\n\nEye doctors often refer to nearsightedness less than -5 or -6 diopters as "common myopia." Nearsightedness of -6 diopters or more is commonly called "high myopia." This distinction is important because high myopia increases a person's risk of developing other eye problems that can lead to permanent vision loss or blindness. These problems include tearing and detachment of the retina, clouding of the lens (cataract), and an eye disease called glaucoma that is usually related to increased pressure within the eye. The risk of these other eye problems increases with the severity of the nearsightedness. The term "pathological myopia" is used to describe cases in which high myopia leads to tissue damage within the eye.
Cataract
MedGen UID:
39462
Concept ID:
C0086543
Disease or Syndrome
A cataract is an opacity or clouding that develops in the crystalline lens of the eye or in its capsule.
Asteroid hyalosis
MedGen UID:
636821
Concept ID:
C0521770
Disease or Syndrome
The presence of small, white vitreous opacities consisting of calcium phosphate and complex, layered lipid deposits.
Retinal thinning
MedGen UID:
762617
Concept ID:
C3549703
Finding
Reduced anteroposterior thickness of the retina. This phenotype can be appreciated by retinal optical coherence tomography (OCT).

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVMultiple epiphyseal dysplasia, Beighton type
Follow this link to review classifications for Multiple epiphyseal dysplasia, Beighton type in Orphanet.

Recent clinical studies

Etiology

Mei Y, Jiang Y, Shen L, Meng Z, Zhang Z, Zhang H
Orphanet J Rare Dis 2024 Mar 12;19(1):116. doi: 10.1186/s13023-024-03089-x. PMID: 38475860Free PMC Article
Leoni C, Tedesco M, Radio FC, Chillemi G, Leone A, Bruselles A, Ciolfi A, Stellacci E, Pantaleoni F, Butera G, Rigante D, Onesimo R, Tartaglia M, Zampino G
Am J Med Genet A 2021 Oct;185(10):3153-3160. Epub 2021 Jun 23 doi: 10.1002/ajmg.a.62399. PMID: 34159694
Chetty M, Roomaney IA, Beighton P
Clin Genet 2021 Jan;99(1):42-52. Epub 2020 Nov 3 doi: 10.1111/cge.13846. PMID: 32901963
Wessels A, Wainwright HC, Beighton P
Pediatr Dev Pathol 2011 Nov-Dec;14(6):496-500. Epub 2011 Oct 10 doi: 10.2350/11-01-0969-CR.1. PMID: 21985323
Anderson IJ, Tsipouras P, Scher C, Ramesar RS, Martell RW, Beighton P
Am J Med Genet 1990 Oct;37(2):272-6. doi: 10.1002/ajmg.1320370223. PMID: 1978986

Diagnosis

Leoni C, Tedesco M, Radio FC, Chillemi G, Leone A, Bruselles A, Ciolfi A, Stellacci E, Pantaleoni F, Butera G, Rigante D, Onesimo R, Tartaglia M, Zampino G
Am J Med Genet A 2021 Oct;185(10):3153-3160. Epub 2021 Jun 23 doi: 10.1002/ajmg.a.62399. PMID: 34159694
Agenbag G, Vorster A, Julius S, Ramesar R, Beighton P
S Afr Med J 2020 Dec 14;111(1):57-60. doi: 10.7196/SAMJ.2020.v111i1.14561. PMID: 33404007
Bieganski T, Beighton P, Lukaszewski M, Bik K, Kuszel L, Wasilewska E, Kozlowski K, Czarny-Ratajczak M
Eur J Med Genet 2017 Oct;60(10):509-516. Epub 2017 Jul 4 doi: 10.1016/j.ejmg.2017.07.004. PMID: 28687525Free PMC Article
Vorster AA, Beighton P, Ramesar RS
Clin Genet 2015 May;87(5):492-5. Epub 2014 May 22 doi: 10.1111/cge.12413. PMID: 24766538
Wessels A, Wainwright HC, Beighton P
Pediatr Dev Pathol 2011 Nov-Dec;14(6):496-500. Epub 2011 Oct 10 doi: 10.2350/11-01-0969-CR.1. PMID: 21985323

Therapy

Kobayasi T
Eur J Dermatol 2004 Jul-Aug;14(4):221-9. PMID: 15319154
Jones CJ, Cummings C, Ball J, Beighton P
S Afr Med J 1984 Dec 15;66(24):907-10. PMID: 6505901

Prognosis

Mei Y, Jiang Y, Shen L, Meng Z, Zhang Z, Zhang H
Orphanet J Rare Dis 2024 Mar 12;19(1):116. doi: 10.1186/s13023-024-03089-x. PMID: 38475860Free PMC Article
Wessels A, Wainwright HC, Beighton P
Pediatr Dev Pathol 2011 Nov-Dec;14(6):496-500. Epub 2011 Oct 10 doi: 10.2350/11-01-0969-CR.1. PMID: 21985323
Sykes B, Ogilvie D, Wordsworth P, Wallis G, Mathew C, Beighton P, Nicholls A, Pope FM, Thompson E, Tsipouras P
Am J Hum Genet 1990 Feb;46(2):293-307. PMID: 1967900Free PMC Article
Beighton P, Spranger J, Versveld G
S Afr Med J 1983 Oct 1;64(15):565-8. PMID: 6623243
Beighton P, Hamersma H, Cremin BJ
S Afr Med J 1979 Apr 21;55(17):659-65. PMID: 462288

Clinical prediction guides

Mei Y, Jiang Y, Shen L, Meng Z, Zhang Z, Zhang H
Orphanet J Rare Dis 2024 Mar 12;19(1):116. doi: 10.1186/s13023-024-03089-x. PMID: 38475860Free PMC Article
Agenbag G, Vorster A, Julius S, Ramesar R, Beighton P
S Afr Med J 2020 Dec 14;111(1):57-60. doi: 10.7196/SAMJ.2020.v111i1.14561. PMID: 33404007
Wessels A, Wainwright HC, Beighton P
Pediatr Dev Pathol 2011 Nov-Dec;14(6):496-500. Epub 2011 Oct 10 doi: 10.2350/11-01-0969-CR.1. PMID: 21985323
Wallis GA, Sykes B, Byers PH, Mathew CG, Viljoen D, Beighton P
J Med Genet 1993 Jun;30(6):492-6. doi: 10.1136/jmg.30.6.492. PMID: 8100856Free PMC Article
Sher C, Ramesar R, Martell R, Learmonth I, Tsipouras P, Beighton P
Am J Hum Genet 1991 Mar;48(3):518-24. PMID: 1671807Free PMC Article

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