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[Specific enzyme diagnosis in mitochondrial myopathies and encephalomyopathies].

作者信息

László A, Sümegi B, Alkonyi I, Horváth E, Sztriha L, Várkonyi A, Zombori J

机构信息

Szent-Györgyi Albert Orvostudományi Egyetem, Gyermekklinika, Szeged.

出版信息

Orv Hetil. 1994 Apr 3;135(14):747-50.

PMID:8170674
Abstract

Mitochondrial enzyme activities (cytochrome c-oxidase = COX, carnitine acyl-transferase = CAT, citrate synthase = CS, lipoamide dehydrogenase = lipDH from the pyruvate-dehydrogenase complex, lactate dehydrogenase = LDH, and malate-dehydrogenase = MDH) were measured from progressive myopathy/encephalomyopathy. Cytochrome oxidase (COX) deficiency was detected from muscle or liver tissues, adult type of COX defectus had been diagnosed in 1 case and infantile type in further 6 cases. The 3 familial atactic children showed decreased activity of carnitine acetyl-transferase, too.

摘要

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