Yacovino Darío A, Gomez Alan, Mayer María Belén, Fay Fabián
Servicio de Neurología, Hospital Dr. Cesar Milstein, Buenos Aires, Argentina. E-mail:
Laboratorio CIBIC, Rosario, Santa Fe, Argentina.
Medicina (B Aires). 2024;84(3):555-559.
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.
小脑性共济失调、神经病和前庭反射消失综合征(CANVAS)是一种迟发性神经退行性疾病。其遗传基础最近在编码复制因子C(RFC1)一个亚基的基因中被确定。我们报告一例62岁女性病例,其有双相性失衡和步态障碍病史,症状起病迅速,随后出现缓慢进行性神经功能恶化。诊断过程具有挑战性,进行了多项检查以排除共济失调的后天性和遗传性病因,最终诊断为迟发性特发性小脑性共济失调。随后,前庭功能测试发现严重的双侧前庭病变。这使得CANVAS被纳入诊断考虑范围,最终通过基因检测(RFC1基因中五核苷酸AAGGG的双等位基因扩增)得以确诊。该病例凸显了这种新描述的遗传疾病及其亚急性表现变体的重要性,强调了客观前庭功能测试在特发性共济失调中对于实现正确诊断以及最终为后代进行遗传咨询的相关性。