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在一个RFC1基因双等位基因重复扩增的家族中,痉挛性咳嗽先于CANVAS表型出现。

Spasmodic cough preceding CANVAS phenotype in a family with biallelic repeat expansions in RFC1.

作者信息

Malaquias Maria João, Mendes Pinto Catarina, Sardoeira Ana, Oliveira Jorge, Parente Freixo João, Aires Silva Ana, Abreu Pedro, Rosado Coelho Cristina, Damásio Joana, Vila-Chã Nuno, Magalhães Marina

机构信息

Neurology Department, Centro Hospitalar Universitário do Porto, Largo do Prof. Abel Salazar, 4099-001, Porto, Portugal.

Neurorradiology Department, Centro Hospitalar Universitário do Porto, Porto, Portugal.

出版信息

Neurol Sci. 2021 Feb;42(2):749-753. doi: 10.1007/s10072-020-04895-4. Epub 2020 Nov 13.

Abstract

Cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS) is a late-onset, multisystem ataxia that remained only clinically defined, until recently, when the discovery of biallelic repeat expansion in the RFC1 gene allowed the genetic link. We describe the first Portuguese familial CANVAS harboring the pathogenic RFC1 expansion. Detail clinical features and course of four affected members are provided. Phenotype characterizations are important as the novel RFC1 mutation is expected to be a major cause of idiopathic late-onset ataxia.

摘要

伴有神经病变和前庭反射消失综合征的小脑共济失调(CANVAS)是一种迟发性多系统共济失调,直到最近发现 RFC1 基因双等位基因重复扩增确定了其遗传联系之前,一直仅在临床上有定义。我们描述了首例携带致病性 RFC1 扩增的葡萄牙家族性 CANVAS。提供了四名受影响成员的详细临床特征和病程。由于预计新的 RFC1 突变将是特发性迟发性共济失调的主要原因,因此表型特征描述很重要。

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