Search on: MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL 
Descriptors Found: 1
Displaying: 1 .. 1  

 1 / 1 DeCS     
Descriptor English:   Muscular Dystrophy, Facioscapulohumeral 
Descriptor Spanish:   Distrofia Muscular Facioescapulohumeral 
Descriptor Portuguese:   Distrofia Muscular Facioescapuloumeral 
Synonyms English:   Facioscapulohumeral Muscular Dystrophy
Landouzy-Dejerine Dystrophy  
Tree Number:   C05.651.534.500.400
C10.668.491.175.500.400
C16.320.577.400
Definition English:   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) 
History Note English:   2000 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications CN congenital
DI diagnosis DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RA radiography
RI radionuclide imaging RT radiotherapy
RH rehabilitation SU surgery
TH therapy US ultrasonography
UR urine VI virology
Record Number:   34192 
Unique Identifier:   D020391 

Occurrence in VHL:
 

Similar:

 
DeCS CID-10 SciELO LILACS LIS