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type
sameAs
notation
  • C05.651.534.500.400
  • C10.668.491.175.500.400
  • C16.320.577.400
alternative label
  • Myopathie facio-scapulo-humérale de Landouzy-Déjerine
  • Maladie de Landouzy-Déjerine
  • Myopathie de Landouzy-Déjerine
  • Atrophy, Facioscapulohumeral
  • Dystrophies, Facioscapulohumeral Muscular
  • FSH Muscular Dystrophy
  • Facioscapulohumeral Atrophy
  • Facioscapulohumeral Muscular Dystrophy
  • Facioscapuloperoneal Muscular Dystrophy
  • Landouzy Dejerine Dystrophy
  • Landouzy-Dejerine Dystrophies
  • Muscular Dystrophies, Facioscapulohumeral
  • Facioscapulohumeral Type Progressive Muscular Dystrophy
  • Progressive Muscular Dystrophy, Facioscapulohumeral Type
  • Atrophies, Facioscapulohumeral
  • Dystrophy, Facioscapulohumeral Muscular
  • Dystrophy, Landouzy-Dejerine
  • Facio-Scapulo-Humeral Dystrophy
  • Landouzy-Dejerine Dystrophy
  • Myopathie facio-scapulo-humérale
  • Dystrophies, Landouzy-Dejerine
  • Facioscapulohumeral Atrophies
  • Facioscapulohumeral Muscular Dystrophies
  • Muscular Dystrophy, Facioscapulohumeral
  • Muscular Dystrophy, Landouzy Dejerine
  • Atrophie facio-scapulo-humérale de Landouzy-Déjerine
preferred label
  • Dystrophie musculaire facio-scapulo-humérale
is in scheme
note
  • 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)
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