Congenital myasthenic syndrome: report of four cases and brief review of literature.
Neurol India
;
2000 Sep; 48(3): 266-71
Artículo
en Inglés
| 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:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Autoanticuerpos
/
Femenino
/
Humanos
/
Masculino
/
Niño
/
Salud de la Familia
/
Adulto
/
Síndromes Miasténicos Congénitos
/
Electrodiagnóstico
Tipo de estudio:
Estudio pronóstico
Idioma:
Inglés
Revista:
Neurol India
Año:
2000
Tipo del documento:
Artículo
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