| Literature DB >> 31049853 |
Maria Thereza Drumond Gama1, Pedro Braga-Neto2,3, Livia Almeida Dutra1, Helena Alessi1, Lilia Alves Maria1, Ary Araripe Gadelha4, Bruno Bertolucci Ortiz4, Ilda Kunii5, Silvia Regina Correia-Silva5, Magnus R Dias da Silva5, Patrick A Dion6, Guy A Rouleau6, Marcondes Cavalcante França7, Orlando G P Barsottini8, José Luiz Pedroso1.
Abstract
SYNE1 gene mutations were identified as a cause of late-onset pure cerebellar syndrome. Non-cerebellar symptoms, including cognitive impairment, were already described in this condition. The aim of this study was to perform a detailed cognitive and psychiatric description of patients with SYNE1 gene mutations. We performed neuropsychological and psychiatric evaluations of six patients with SYNE1 ataxia and compared their performance with 18 normal controls paired for age and education level. SYNE1 ataxia patients present cognitive dysfunction, characterized by impairment in attention and processing speed domains. Otherwise, the psychiatric assessment reported low levels of overall behavioral symptoms with only some minor anxiety-related complaints. Although this is a small sample of patients, these results suggest that SYNE1 ataxia patients may represent a model to investigate effects of cerebellar degeneration in higher hierarchical cognitive functions. For further studies, abstract thinking impairment in schizophrenia may be related to dysfunction in cerebellum pathways.Entities:
Keywords: Cerebellar cognitive affective syndrome; Cognitive impairment; Hereditary ataxias; SYNE1 mutations
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Year: 2019 PMID: 31049853 DOI: 10.1007/s12311-019-01033-5
Source DB: PubMed Journal: Cerebellum ISSN: 1473-4222 Impact factor: 3.847