Emery-Dreifuss Muscular Dystrophy 5, Autosomal Dominant

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WHO-ICD-10 version:2010

Diseases of the nervous system

Diseases of myoneural junction and muscle

OMIM Number

612999

Gene Map Locus

14q23.2

Description

Emery-Dreifuss muscular dystrophy is a degenerative myopathy characterized by weakness and atrophy of muscle without involvement of the nervous system. Flexion deformities of the elbows dating from early childhood, mild pectus excavatum, signs of cardiac involvement and absence of muscle pseudohypertrophy, involvement of the forearm muscles, and mental retardation distinguish the Emery-Dreifuss form (EDMD1) from the Becker form. Emery-Dreifuss muscular dystrophy-5 (EDMD5) is caused by heterozygous mutation in the SYNE2 gene

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
612999.1LebanonUnknown Global developmental delayNM_015180.5:c.19372G>AHeterozygousAutosomal, DominantJalkh et al. 2019
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