Congenital myasthenic syndrome: report of four cases and brief review of literature.
Neurol India
; 2000 Sep; 48(3): 266-71
Article
em En
| 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.
Texto completo:
1
Índice:
IMSEAR
Assunto principal:
Autoanticorpos
/
Feminino
/
Humanos
/
Masculino
/
Criança
/
Saúde da Família
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Adulto
/
Síndromes Miastênicas Congênitas
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Eletrodiagnóstico
Tipo de estudo:
Prognostic_studies
Idioma:
En
Revista:
Neurol India
Ano de publicação:
2000
Tipo de documento:
Article