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Muscular Dystrophy, Facioscapulohumeral

More information in Books or onNLM PubMed
Definition: An autosomal dominant degenerative muscle disease characterized by slowly progressive weakness of the muscles of the face, upper-arm, and shoulder girdle. The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation. This tends to be followed by facial weakness, primarily involving the orbicularis oris and orbicularis oculi muscles. (Neuromuscul Disord 1997;7(1):55-62; Adams et al., Principles of Neurology, 6th ed, p1420)      Other names Muscular Dystrophies, Facioscapulohumeral; Landouzy-Dejerine Dystrophies; Landouzy Dejerine Dystrophy; Facioscapulohumeral Muscular Dystrophies; Facioscapulohumeral Atrophies; Dystrophy, Landouzy-Dejerine; Dystrophy, Facioscapulohumeral Muscular; Dystrophies, Landouzy-Dejerine; Dystrophies, Facioscapulohumeral Muscular; Atrophy, Facioscapulohumeral; Atrophies, Facioscapulohumeral; Progressive Muscular Dystrophy, Facioscapulohumera; Facioscapulohumeral Type Progressive Muscular Dyst; Facioscapulohumeral Atrophy; Landouzy-Dejerine Dystrophy; Facioscapulohumeral Muscular Dystrophy
 
SubstanceCAS Registry & nameCategoriesSource
Facioscapulohumeral muscular dystrophy 1a  0   *Muscular Dystrophy, Facioscapulohumeral.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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