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Rehabilitation Practice and Science

Translated Title

先天性桿狀肌病:病例報告

Abstract

A 5 year-old boy had non-progressive myopathy since 2 years of age. Muscle enzymes were normal. Electromyography showed a myopathic feature. Prominantly disseminated nemaline bodies and predominant type I muscle fibers were found in muscle biopsy specimen. The clinical and morphological findings supported the existence of a rare form of congenital myopathy.

Language

English

First Page

186

Last Page

191

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