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首例 RANBP2 双等位基因突变伴严重急性坏死性脑病表型。

First case with RANBP2 biallelic mutation and severe acute necrotizing encephalopathy phenotype.

机构信息

Department of Medical Genetics, Faculty of Medicine, Istanbul Medipol University, Istanbul, Turkey; Genetic Diseases Assessment Center, Istanbul Medipol University, Istanbul, Turkey.

Genetic Diseases Assessment Center, Istanbul Medipol University, Istanbul, Turkey.

出版信息

Clin Neurol Neurosurg. 2022 Oct;221:107418. doi: 10.1016/j.clineuro.2022.107418. Epub 2022 Aug 23.

Abstract

Familial acute necrotizing encephalopathy (ANE) is a rapidly progressive encephalopathy that can occur after common viral infections at different stages of life. The clinical findings of 2 siblings diagnosed with ANE were shared and the whole-exome-sequencing study of the index case was performed. It was confirmed by the Sanger method. We found the RANBP2 gene p.I656V variant homozygous in the index case. We found the variant in the parents as heterozygous. We argue that biallelic mutations in the RANBP2 gene may result in ANE with early onset and severe prognosis by increasing penetrance.

摘要

家族性急性坏死性脑病(ANE)是一种在生命不同阶段常见病毒感染后可能发生的快速进展性脑病。我们分享了 2 名被诊断为 ANE 的兄弟姐妹的临床发现,并对索引病例进行了全外显子组测序研究。该研究通过 Sanger 方法得到证实。我们发现索引病例 RANBP2 基因 p.I656V 杂合突变。该变异在父母中为杂合子。我们认为 RANBP2 基因的双等位基因突变可能通过增加外显率导致早发性和严重预后的 ANE。

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