Case Report: Late-Onset Autosomal Recessive Cerebellar Ataxia Associated With SYNE1 Mutation in a Chinese Family

• Published in: Frontiers in genetics 2022-02, Vol.13, p.795188
• Main Authors: Qian, Nannan, Wei, Taohua, Yang, Wenming, Wang, Jiuxiang, Zhang, Shijie, Jin, Shan, Dong, Wei, Hao, Wenjie, Yang, Yue, Huang, Ru
• Format: Article
• Language: English
• Subjects: ARCA-1; autosomal recessive cerebellar ataxia; case report; Genetics; SCAR8; SYNE1 ataxia; SYNE1 gene
• ISSN: 1664-8021; 1664-8021
• DOI: 10.3389/fgene.2022.795188

Autosomal recessive cerebellar ataxia type 1 (ARCA-1), also known as autosomal recessive spinocerebellar ataxia type 8 (SCAR8), is caused by spectrin repeat containing nuclear envelope protein 1 ( ) gene mutation. Nesprin-1, encoded by , is widely expressed in various tissues, especially in the striated muscle and cerebellum. The destruction of Nesprin-1 is related to neuronal and neuromuscular lesions. It has been reported that gene variation is associated with Emery-Dreifuss muscular dystrophy type 4, arthrogryposis multiplex congenita, SCAR8, and dilated cardiomyopathy. The clinical manifestations of SCAR8 are mainly characterized by relatively pure cerebellar ataxia and may be accompanied by upper and/or lower motor neuron dysfunction. Some affected people may also display cerebellar cognitive affective syndrome. It is conventionally held that the age at the onset of SCAR8 is between 6 and 42 years (the median age is 17 years). Here, we report a pedigree with SCAR8 where the onset age in the proband is 48 years. This case report extends the genetic profile and clinical features of SCAR8. A new pathogenic site (c.7578del; p.S2526Sfs*8) located in , which is the genetic cause of the patient, was identified via whole exome sequencing (WES).