Literature DB >> 15008504

Cognitive impairment in SCA-19.

H Jurgen Schelhaas1, Bart P C van de Warrenburg, Gerard Hageman, Elly E Ippel, Monique van Hout, Berry Kremer.   

Abstract

The autosomal dominant cerebellar ataxias (ADCAs) are a heterogeneous group of neurodegenerative disorders characterised by progressive cerebellar dysfunction in combination with various associated features. Since 1993, ADCAs have been increasingly characterised in terms of their genetic mutation and are currently referred to as spinocerebellar ataxias (SCAs). The discovery of genetic abnormalities offers the opportunity to study the possible interaction between the identified gene mutation and cognitive function. In this study, we focus on the neuropsychological abnormalities in a Dutch ADCA family, in which a new locus was recently identified (SCA-19). The family members showed frontal-executive dysfunction, with global cognitive impairment occurring in some of the more severely affected patients. Interestingly, the neuropsychological profile of this new family seems to overlap that of individuals with various other SCAs. Apparently, similar pattern of neuronal degeneration in various SCA subtypes accounts for the neuropsychological dysfunction, which is thus not genotype specific.

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Year:  2003        PMID: 15008504

Source DB:  PubMed          Journal:  Acta Neurol Belg        ISSN: 0300-9009            Impact factor:   2.396


  7 in total

Review 1.  Clinical, psychological, and genetic characteristics of spinocerebellar ataxia type 19 (SCA19).

Authors:  H Jurgen Schelhaas; Bart P C van de Warrenburg
Journal:  Cerebellum       Date:  2005       Impact factor: 3.847

Review 2.  Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders.

Authors:  Erin E Robertson; Deborah A Hall; Andrew R McAsey; Joan A O'Keefe
Journal:  Clin Neuropsychol       Date:  2016-08       Impact factor: 3.535

3.  Novel De Novo KCND3 Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and Dystonia.

Authors:  Masanori Kurihara; Hiroyuki Ishiura; Takuya Sasaki; Juuri Otsuka; Toshihiro Hayashi; Yasuo Terao; Takashi Matsukawa; Jun Mitsui; Juntaro Kaneko; Kazutoshi Nishiyama; Koichiro Doi; Jun Yoshimura; Shinichi Morishita; Jun Shimizu; Shoji Tsuji
Journal:  Cerebellum       Date:  2018-04       Impact factor: 3.847

4.  Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19.

Authors:  Martin Paucar; Åsa Bergendal; Peter Gustavsson; Magnus Nordenskjöld; José Laffita-Mesa; Irina Savitcheva; Per Svenningsson
Journal:  Cerebellum       Date:  2018-08       Impact factor: 3.847

Review 5.  Cognition in hereditary ataxia.

Authors:  Katrin Bürk
Journal:  Cerebellum       Date:  2007       Impact factor: 3.648

6.  Cognitive impairment in Spinocerebellar ataxia type 10.

Authors:  Adriana Moro; Hélio Afonso Ghizoni Teive
Journal:  Dement Neuropsychol       Date:  2016 Oct-Dec

Review 7.  Cognitive dysfunction in spinocerebellar ataxias.

Authors:  Helio Afonso Ghizoni Teive; Walter Oleschko Arruda
Journal:  Dement Neuropsychol       Date:  2009 Jul-Sep
  7 in total

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