Congenital myasthenic syndrome: report of four cases and brief review of literature.
Neurol India
;
2000 Sep; 48(3): 266-71
Article
Dans Anglais
| IMSEAR
| ID: sea-121040
ABSTRACT
The term 'congenital myasthenic syndrome' (CMS) encompasses a number of heterogeneous disorders characterised by myasthenic symptoms since birth, usually with positive family history and absence of acetyl choline receptor antibodies. Recent advances in electrophysiology and ultrastructural analysis of neuromuscular junction have made it possible to identify the various defects underlying these disorders. We report four cases of CMS, with a review of literature.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Autoanticorps
/
Femelle
/
Humains
/
Mâle
/
Enfant
/
Santé de la famille
/
Adulte
/
Syndromes myasthéniques congénitaux
/
Électrodiagnostic
Type d'étude:
Étude pronostique
langue:
Anglais
Texte intégral:
Neurol India
Année:
2000
Type:
Article
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