Muscular Dystrophy, Facioscapulohumeral [facioskapulohumerální svalová dystrofie]

topical
19
Terms

dystrofie Landouzyho-Dejerineova typu
facioskapulohumerální muskulární dystrofie
svalová dystrofie facioskapulohumerální

 

Facio-Scapulo-Humeral Dystrophy
Facioscapulohumeral Atrophy
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

Persistent link   https://www.medvik.cz/link/D020391
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)

DUI
D020391 MeSH Browser
CUI
M0328187
Previous indexing
Muscular Dystrophies (1966-1999)
History note
2000
Public note
2000

C Diseases
C05.651.534.500 Muscular Dystrophies 141
C05.651.534.500.074 Distal Myopathies 3
C05.651.534.500.300 Muscular Dystrophy, Duchenne 136
C05.651.534.500.500 Myotonic Dystrophy 96
C10.668.491 Muscular Diseases 557
C10.668.491.175.500 Muscular Dystrophies 141
C10.668.491.175.500.074 Distal Myopathies 3
C10.668.491.175.500.112 Glycogen Storage Disease Type VII
C10.668.491.175.500.149 Muscular Dystrophies, Limb-Girdle 22
C10.668.491.175.500.300 Muscular Dystrophy, Duchenne 136
C10.668.491.175.500.350 Muscular Dystrophy, Emery-Dreifuss 18
C10.668.491.175.500.450 Muscular Dystrophy, Oculopharyngeal 3
C10.668.491.175.500.500 Myotonic Dystrophy 96
C16.320.577 Muscular Dystrophies 141
C16.320.577.074 Distal Myopathies 3
C16.320.577.300 Muscular Dystrophy, Duchenne 136
C16.320.577.500 Myotonic Dystrophy 96
C16.320.577.750 Walker-Warburg Syndrome 4

Facioscapulohumeral Muscular Dystrophy 1B Disease MeSH Browser

Facioscapulohumeral muscular dystrophy 1a Disease MeSH Browser

Muscular Dystrophy, Scapulohumeral Disease MeSH Browser

Myopathy with Storage of Glycoproteins and Glycosaminoglycans Disease MeSH Browser