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Mitochondrial myopathy with respiratory muscle involvement: a case report

By J. A. Levy, Ana M. Tsanaclis, P. A. P. Saraiva, Carmen C. Mion and Paulo N. B. Salum

Abstract

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

Topics: Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Internal medicine, RC31-1245, Medicine, R
Publisher: Academia Brasileira de Neurologia (ABNEURO)
Year: 1983
DOI identifier: 10.1590/S0004-282X1983000100008
OAI identifier: oai:doaj.org/article:8417f4cf2dae49c484934f3fe78dfc72
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