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[A case of mitochondrial enzymopathy].

作者信息

Parafiniuk W, Kowalczyk K, Bajko J, Sycz K

机构信息

Zakładu Patomorfologii Klinicznej Instytutu Patologii PAN w Szczecinie.

出版信息

Neurol Neurochir Pol. 1988 May-Jun;22(3):260-3.

PMID:2975767
Abstract

A case of mitochondrial enzymopathy, called also ophthalmoplegia plus, was observed in a 31-year-old man. Histoenzymatic investigations demonstrated in the myocytes decreased and irregularity of reactions for succinic dehydrogenase, tetrazole reductase and mitochondrial ATPase. In electron microscopy paracrystalline structures, lamellar bodies and concentrically condensed cristae were seen in the mitochondria, and increased glycogen stores outside the mitochondria.

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