Search on: MYOTONIA CONGENITA 
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Descriptor English:   Myotonia Congenita 
Descriptor Spanish:   Miotonía Congénita 
Descriptor Portuguese:   Miotonia Congênita 
Synonyms English:   Thomsen Disease
Becker Generalized Myotonia
Myotonia, Generalized, Becker  
Tree Number:   C05.651.662.500
C10.574.500.545
C10.668.491.606.500
C16.320.400.540
Definition English:   A dominantly inherited muscle disease that begins in early childhood and is characterized by severe myotonia (delayed relaxation of a muscle) after forceful voluntary contractions. Muscular hypertrophy is common and myotonia may impair ambulation and other movements. Myotonia typically becomes less severe with repetitive voluntary contractions of the affected muscles. Generalized myotonia (of Becker) is an autosomal recessive variant of myotonia congenita that may feature more severe myotonia and muscle wasting. (From Adams et al., Principles of Neurology, 6th ed, pp1476-7; Joynt, Clinical Neurology, 1997, Ch53, p18) 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications 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
VE veterinary VI virology
Record Number:   9415 
Unique Identifier:   D009224 

Occurrence in VHL:
 

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