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伴有线粒体复合体I缺乏的坏死性脑病和巨头畸形

Necrotizing encephalopathy and macrocephaly with mitochondrial complex I deficiency.

作者信息

Feillet F, Mousson B, Grignon Y, Leonard J V, Vidailhet M

机构信息

Service de Médecine Infantile III, Hôpital d'Enfants, Nancy, France.

出版信息

Pediatr Neurol. 1999 Apr;20(4):305-8. doi: 10.1016/s0887-8994(98)00162-3.

Abstract

A neonate presented in the first weeks after birth with vomiting. He was unresponsive, with hypotonia, macrocephaly, and lactic acidosis. The cranial computed tomographic scan revealed a hypodense brain, with increased brain volume and extensive cerebral edema. He died at 6 weeks of age; postmortem examination revealed necrotizing encephalopathy with marked brain edema, spongiosis, thalamic necrosis, and basal ganglia calcifications. Enzyme studies of the mitochondrial respiratory chain revealed complex I deficiency in both muscle and liver.

摘要

一名新生儿在出生后的头几周出现呕吐症状。他反应迟钝,肌张力减退,头大,并有乳酸酸中毒。头颅计算机断层扫描显示脑密度减低,脑容量增加,并有广泛的脑水肿。他在6周龄时死亡;尸检显示为坏死性脑病,伴有明显的脑水肿、海绵状变性、丘脑坏死和基底神经节钙化。线粒体呼吸链的酶学研究显示肌肉和肝脏中均存在复合体I缺乏。

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