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肥厚型心肌病伴发随意肌线粒体肌病及先天性白内障。

Hypertrophic cardiomyopathy associated with a mitochondrial myopathy of voluntary muscles and congenital cataract.

作者信息

Sengers R C, Stadhouders A M, van Lakwijk-Vondrovicova E, Kubat K, Ruitenbeek W

出版信息

Br Heart J. 1985 Nov;54(5):543-7. doi: 10.1136/hrt.54.5.543.

Abstract

Structurally abnormal mitochondria were found in skeletal muscle cells from a woman with hypertrophic cardiomyopathy and myopathy of voluntary muscles associated with congenital cataracts. Moderate exercise resulted in lactic acidosis. Oxidation of pyruvate and other substrates and the production of adenosine triphosphate were normal in vitro. A younger brother of the patient had had congenital cataract and had died from hypertrophic obstructive cardiomyopathy.

摘要

在一名患有肥厚型心肌病和伴有先天性白内障的随意肌病的女性的骨骼肌细胞中发现了结构异常的线粒体。适度运动导致了乳酸性酸中毒。丙酮酸和其他底物的氧化以及三磷酸腺苷的产生在体外是正常的。该患者的一个弟弟患有先天性白内障,并死于肥厚性梗阻性心肌病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b27/481944/aa1e6090e43f/brheartj00119-0090-a.jpg

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