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Muscular Dystrophy, Facioscapulohumeral  

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Tipo

  • mesh:Descriptor

Definición

  • 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)

Concepto genérico

Etiquetas alternativas

  • Facioscapulohumeral Atrophy
  • Facio-Scapulo-Humeral Dystrophy
  • Facioscapulohumeral Muscular Dystrophy
  • Facioscapulohumeral Type Progressive Muscular Dystrophy
  • Facioscapuloperoneal Muscular Dystrophy
  • FSH Muscular Dystrophy
  • Landouzy-Dejerine Dystrophy
  • Muscular Dystrophy, Landouzy Dejerine
  • Progressive Muscular Dystrophy, Facioscapulohumeral Type

En otras lenguas

  • francés

  • Atrophie facio-scapulo-humérale de Landouzy-Déjerine
  • Maladie de Landouzy-Déjerine
  • Myopathie de Landouzy-Déjerine
  • Myopathie facio-scapulo-humérale
  • Myopathie facio-scapulo-humérale de Landouzy-Déjerine

URI

http://data.loterre.fr/ark:/67375/JVR-SPLZTKZ1-G

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