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区分散发性肌萎缩侧索硬化症和家族性肌萎缩侧索硬化症的困难。

Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis.

作者信息

Orrell R W, Habgood J, Rudge P, Lane R J, de Belleroche J S

机构信息

Department of Biochemistry, Charing Cross and Westminister Medical School, London, England.

出版信息

Ann Neurol. 1996 Jun;39(6):810-2. doi: 10.1002/ana.410390620.

Abstract

Mutations of the copper/zinc superoxide dismutase (SOD-1) gene are present in around 20% of patients with a family history of amyotrophic lateral sclerosis. The finding of these mutations in patients with sporadic amyotrophic lateral sclerosis is rare. We describe a family with amyotrophic lateral sclerosis associated with the SOD-1 mutation Asp 101 Asn. This mutation was previously described as occurring in a patient with sporadic disease. We discuss the difficulties in defining truly sporadic amyotrophic lateral sclerosis, and the consequent implications on the neurogenetic advice given to other family members.

摘要

约20%有肌萎缩侧索硬化家族史的患者存在铜/锌超氧化物歧化酶(SOD - 1)基因突变。在散发性肌萎缩侧索硬化患者中发现这些突变的情况较为罕见。我们描述了一个与SOD - 1突变Asp 101 Asn相关的肌萎缩侧索硬化家族。该突变此前曾在一名散发性疾病患者中被描述过。我们讨论了定义真正的散发性肌萎缩侧索硬化的困难,以及由此对给予其他家庭成员的神经遗传学建议产生的影响。

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