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荷斯坦-弗里生犊牛瓜氨酸血症的超微结构研究结果。

Ultrastructural findings in citrullinaemia in Holstein-Friesian calves.

作者信息

Harper P A, Healy P J, Dennis J A, Martin A B

机构信息

Veterinary Laboratories, New South Wales Department of Agriculture, Glenfield, Australia.

出版信息

Acta Neuropathol. 1988;76(3):306-10. doi: 10.1007/BF00687780.

Abstract

Ultrastructural findings in the brains and livers of four calves affected with citrullinaemia due to a hereditary deficiency of the urea cycle enzyme arginosuccinate synthetase are described. The calves were affected in the 1st week of life with severe neurological disease characterised by depression, head pressing, stupor, convulsions and coma, accompanied by marked elevation of plasma citrulline and increasing plasma ammonia levels. Lesions included mild to moderate diffuse astroglial oedema in the cerebrocortical grey matter, and mild to severe hepatocellular hydropic change. The onset of the severe neurological signs was correlated with increasing levels of plasma ammonia, and the cerebral lesions were considered consistent with a bovine hyperammonaemic encephalopathy.

摘要

本文描述了四只患有瓜氨酸血症的犊牛的大脑和肝脏的超微结构发现,这些犊牛因遗传性尿素循环酶精氨琥珀酸合成酶缺乏而患病。犊牛在出生后第一周出现严重的神经疾病,表现为精神沉郁、头部抵压、昏迷、惊厥和昏迷,同时伴有血浆瓜氨酸显著升高和血浆氨水平升高。病变包括大脑皮质灰质轻度至中度弥漫性星形胶质细胞水肿,以及轻度至重度肝细胞水样变性。严重神经症状的出现与血浆氨水平升高相关,脑部病变被认为与牛高氨血症性脑病一致。

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