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Rev Med Interne ; 31(1): 23-8, 2010 Jan.
Article in French | MEDLINE | ID: mdl-19828214

ABSTRACT

Autoantibodies to glutamic acid decarboxylase (GAD), originally identified in the stiff-person syndrome, are also associated with rare cases of therapy-resistant epilepsy and sporadic cerebellar ataxia. The association of GAD antibodies with these three syndromes and other auto-immune diseases, particularly type 1 diabetes mellitus, argues for their auto-immune origin. Anti-GAD antibodies inhibit GABAergic circuits inducing a neuronal hyper-excitability that seems to be responsible for these three syndromes. However, an additional mechanism seems to be involved in the degenerative component of the cerebellar ataxia associated with anti-GAD antibodies. A more accurate diagnosis and the study of neuropathological cases are necessary to document the different mechanisms implicated in these neurological disorders.


Subject(s)
Autoantibodies/immunology , Glutamate Decarboxylase/immunology , Nervous System Diseases/immunology , Stiff-Person Syndrome/immunology , Humans
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