[The association of the Eaton-Lambert myasthenic syndrome and subacute cerebellar degeneration of nonparaneoplastic origin]

Abstract

A 52-year-old male with Eaton-Lambert syndrome associated to seven years subacute cerebellar degeneration of non paraneoplastic origin is presented. Immunosuppressive treatment with azathioprine allowed the neuromuscular symptoms to be controlled although no appreciable effects were observed in the cerebellar symptoms which remained stable.