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dystrofia svalová facioskapulohumerálna
Č. záznamu d020391 Dátum 06.06.2025 Typ M Tematický termín dystrofia svalová facioskapulohumerálna Iný termín Angličtina (Pseudonym) Facioscapulohumeral Muscular Dystrophy
Angličtina (Pseudonym) Landouzy-Dejerine Dystrophy
Slovenčina (Pseudonym) Landouzyho-Déjerineova dystrofia
MDT C05.651.534.500.400C10.668.491.175.500.400C16.320.577.400 Poznámka 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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