[亚急性共济失调伴有小脑共济失调、神经病变和前庭反射障碍(CANVAS)]。

IF 0.6 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Medicina-buenos Aires Pub Date : 2024-01-01
Darío A Yacovino, Alan Gomez, María Belén Mayer, Fabián Fay
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引用次数: 0

摘要

小脑共济失调、神经病变和前庭反射综合征(CANVAS)是一种晚发型神经退行性疾病。其遗传基础最近在编码复制因子 C(RFC1)亚基的基因中被确定。我们介绍了一例 62 岁女性的病例,她曾有过失衡和步态障碍的双相表现,症状迅速出现,随后神经系统缓慢、进行性恶化。诊断过程极具挑战性,为了排除后天获得性和遗传性共济失调的病因,她进行了大量检查,最终被诊断为晚发性特发性小脑共济失调。随后,前庭功能测试发现了严重的双侧前庭病。因此,考虑将 CANVAS 列入诊断范围,并最终通过基因检测(RFC1 基因中五位核苷酸 AAGGG 的双偶联扩增)证实了这一诊断。该病例凸显了这种新描述的遗传病及其亚急性表现变异的重要性,强调了对特发性共济失调患者进行客观前庭功能测试以获得正确诊断并最终为后代提供遗传咨询的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Subacute ataxia associated with cerebellar ataxia, neuropathy and vestibular areflexia (CANVAS)].

Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome (CANVAS) is a late onset neurodegenerative disorder. Its genetic basis has recently been identified in the gene encoding a subunit of the Replication Factor C (RFC1). We present the case of a 62-year-old woman who experienced a history of a biphasic presentation of imbalance and gait disorders, with rapid onset of symptoms followed by slow and progressive neurological deterioration. The diagnostic process was challenging, and numerous tests were conducted to rule out acquired and genetic causes of ataxia, leading to a diagnosis of late-onset idiopathic cerebellar ataxia. Subsequently, vestibular function tests identified severe bilateral vestibulopathy. This led to considering CANVAS among the diagnoses, which was ultimately confirmed through genetic testing (biallelic expansion of the pentanucleotide AAGGG in the RFC1 gene). This case highlights the importance of this new described genetic disease and its subacute presentation variant, emphasizing the relevance of objective vestibular function tests in idiopathic ataxias to achieve proper diagnosis and eventual genetic counseling for offspring.

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来源期刊
Medicina-buenos Aires
Medicina-buenos Aires 医学-医学:内科
CiteScore
1.30
自引率
12.50%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Information not localized
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