Ullrich congenital muscular dystrophy 1B

Alternative Names

  • UCMD1B
  • Ullrich congenital muscular dystrophy 1A/1B, Digenic
  • UCMD1A/1B, Digenic
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WHO-ICD-10 version:2010

Diseases of the nervous system

Diseases of myoneural junction and muscle

OMIM Number

620727

Mode of Inheritance

Autosomal dominant Autosomal recessive

Gene Map Locus

21q22.3

Description

Ullrich congenital muscular dystrophy-1 (UCMD1) is characterized by generalized muscle weakness and striking hypermobility of distal joints in conjunction with variable contractures of more proximal joints and normal intelligence. Additional findings may include kyphoscoliosis, protruded calcanei, and follicular hyperkeratosis. Some patients manifest at birth and never achieve independent ambulation, whereas others maintain ambulation into adulthood. Progressive scoliosis and deterioration of respiratory function is a typical feature. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
620727.G.1Saudi ArabiaYes Joint hypermobility; Generalized hypoton...NM_001849.4:c.1459-63G>AHomozygousAutosomal, RecessiveAlazami et al, 2016 3 patients - proband...
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