Muscular Dystrophy, Facioscapulohumeral [facioskapulohumerální svalová dystrofie]
- Terms
-
dystrofie Landouzyho-Dejerineova typu
facioskapulohumerální muskulární dystrofie
svalová dystrofie facioskapulohumerální
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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
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
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications 2
- CN
- congenital
- DI
- diagnosis 7
- DG
- diagnostic imaging 1
- DH
- diet therapy 1
- DT
- drug therapy 2
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 1
- EH
- ethnology
- ET
- etiology 2
- GE
- genetics 9
- HI
- history
- IM
- immunology 1
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology
- PP
- physiopathology 1
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 2
- UR
- urine
- VI
- virology
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