Literature DB >> 31423897

Cognitive characterization of SCAR10 caused by a homozygous c.132dupA mutation in the ANO10 gene.

Antonieta Nieto1, Javier Pérez-Flores1, Marc Corral-Juan2, Antoni Matilla-Dueñas2, Francisco Martínez-Burgallo3, Fernando Montón4.   

Abstract

Autosomal recessive spinocerebellar ataxia type 10 (SCAR10) caused by a homozygous c.132dupA mutation in the anoctamin 10 gene is infrequent and little is known about its cognitive profile. Three siblings (1 male) with this mutation were assessed with a neuropsychological battery measuring multiple cognitive domains. The deficits observed in one patient were in executive functions whereas the other two patients showed deficits in practically all the functions. Cognitive impairment seems to be a characteristic of the SCAR10 produced by this mutation, with a range from mild impairment, especially involving prefrontal systems, to a severe cognitive impairment suggesting widespread cerebral involvement.

Entities:  

Keywords:  gene; SCAR10 cognitive impairment; autosomal recessive spinocerebellar ataxia; cerebellum

Mesh:

Substances:

Year:  2019        PMID: 31423897     DOI: 10.1080/13554794.2019.1655064

Source DB:  PubMed          Journal:  Neurocase        ISSN: 1355-4794            Impact factor:   0.881


  2 in total

Review 1.  ANO10 Function in Health and Disease.

Authors:  Androniki Chrysanthou; Antonis Ververis; Kyproula Christodoulou
Journal:  Cerebellum       Date:  2022-06-01       Impact factor: 3.847

2.  Autosomal Recessive Spinocerebellar Ataxia Type 10: A Report of a New Case in Japan.

Authors:  Izumi Aida; Tetsuo Ozawa; Kentaro Ohta; Hidehiko Fujinaka; Kiyoe Goto; Takashi Nakajima
Journal:  Intern Med       Date:  2022-02-01       Impact factor: 1.282

  2 in total

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