Mitochondrial myopathy with respiratory muscle involvement: a case report

A case of a 10-year-old patient with a benign congenital myopathy, suddenly aggravated because of an accentuated deficit in respiratory muscles is reported. The institution of assisted respiration at night allowed the patient to return to her daily activities. Examination of muscular biopsy with ultra-microscope permitted the diagnosis of mitochondrial myopathy.

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Bibliographic Details
Main Authors: Levy,J. A., Tsanaclis,Ana M., Saraiva,P. A. P., Mion,Carmen C., Salum,Paulo N. B.
Format: Digital revista
Language:English
Published: Academia Brasileira de Neurologia - ABNEURO 1983
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1983000100008
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