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J Korean Neurol Assoc. 1984 Dec;2(2):208-216. Korean. Case Report.
Suh MW , Lee KH , Rho JK , Myong HJ .
Department of Neurology, Seoul National University.
Abstract

The authors encountered 2 siblings who showed progressive ophthalmoplegia and bulbar palsy. The patients were studied with various laboratory aids and thought to be as oculopharyngeal muscular dystrophy. The oculopharyngeal muscular dystrophy is a rare form of muscular dystrophy. The authors present the cases as familial oculopharyngeal muscular dystrophy.

Copyright © 2019. Korean Association of Medical Journal Editors.