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
Recommended Citation
Chang, Chein-Wei; Lien, I-Nan; Wang, Pen-June; Huang, Sho-Fen; and Hsu, Hey-Chi
(1990)
"Nemaline Myopathy: A casereport,"
Rehabilitation Practice and Science: Vol. 18:
Iss.
1, Article 25.
DOI: https://doi.org/10.6315/3005-3846.1800
Available at:
https://rps.researchcommons.org/journal/vol18/iss1/25