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成人过氧化物酶体酰基辅酶 A 氧化酶缺乏伴小脑和脑干萎缩。

Adult peroxisomal acyl-coenzyme A oxidase deficiency with cerebellar and brainstem atrophy.

机构信息

Laboratory Genetic Metabolic Diseases, F0-220, Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.

出版信息

J Neurol Neurosurg Psychiatry. 2010 Mar;81(3):310-2. doi: 10.1136/jnnp.2009.176255.

Abstract

Peroxisomal acyl-coenzyme A oxidase deficiency (formerly also called pseudoneonatal adrenoleucodystrophy) is a disorder of peroxisomal fatty acid oxidation with a severe presentation. Most patients present at birth or in early infancy, and the mean age of death was 5 years in a recently published cohort of 22 patients. Brain imaging shows a progressive leucodystrophy. The authors report here the first adult patients (two siblings, 52 and 55 years old) with peroxisomal acyl-coenzyme A oxidase deficiency with a remarkably mild clinical presentation. Magnetic resonance brain imaging revealed profound atrophy of the brainstem and cerebellum.

摘要

过氧化物酶体酰基辅酶 A 氧化酶缺乏症(以前也称为假性新生儿肾上腺脑白质营养不良)是一种过氧化物体脂肪酸氧化的紊乱,表现严重。大多数患者在出生时或婴儿早期发病,在最近发表的 22 例患者队列中,平均死亡年龄为 5 岁。脑影像学显示进行性脑白质营养不良。作者在此报告首例过氧化物体酰基辅酶 A 氧化酶缺乏症的成年患者(两名兄弟姐妹,52 岁和 55 岁),临床表现极为轻微。磁共振脑成像显示脑干和小脑明显萎缩。

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