Myotonia Dystrophica: A Case Report / 대한정형외과학회잡지
The Journal of the Korean Orthopaedic Association
;
: 195-199, 1985.
Article
Dans Coréen
| WPRIM
| ID: wpr-768283
ABSTRACT
Myotonia dystrophica(Synonym Myotonia atrophica, Dystrophia myotonia, Steinert's disease) is a autosomal dominant hereditary multisystemic disorder involving several organs besides skeletal muscle, and commonly called with myotonia congenita, paramyotonia congenita as myotonia. Although most cases are of adult onset, where a mother has the disease, neonatal dystrophia myotonia can occur in her offspring. The main feature is a steadily progressive muscle dystrophy, complicated by myotonia, which is a failure of muscles to relax normally after a forceful contraction. Steinert in 1909 was the first to report the finding of atrophic testes and baldness in patients with myotonia dystrophica, and the other clinical feature of myotonia dystrophica were reported by many authors after that time. We are reporting a case of myotonia dystrophica, which showing familial history with brief review of literature.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Testicule
/
Muscles squelettiques
/
Troubles myotoniques
/
Alopécie
/
Mères
/
Muscles
/
Myotonie
/
Dystrophie myotonique
/
Myotonie congénitale
Limites du sujet:
Adulte
/
Humains
langue:
Coréen
Texte intégral:
The Journal of the Korean Orthopaedic Association
Année:
1985
Type:
Article
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