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Chorea-acanthocytosis: Report of two Brazilian cases. Movement disorders : official journal of the Movement Disorder Society [Mov Disord] Journal article

 
TitleChorea-acanthocytosis: Report of two Brazilian cases.
Author(s)Rodrigues GR, Walker RH, Bader B, Danek A, Marques W, Tumas V 
InstitutionDepartment of Neurology, Ribeirao Preto School of Medicine, Ribeirao Preto, Brazil.
SourceMov Disord 2008 Sep 10.
AbstractChorea-acanthocytosis (ChAc) is a neurodegenerative disorder characterized by chorea, neuropsychiatric disturbances and acanthocytosis, caused by mutations of VPS13A. This gene produces the protein chorein which is absent in patients with ChAc on Western blot assay. We report the first two Brazilian patients with ChAc confirmed by chorein detection. Patient 1 is a 36-year-old man with chorea, epilepsy, myopathy, and suicidal ideation. Patient 2 is a 60-year-old woman with a 30 year history of psychiatric disturbances, epilepsy, choreic movements, and myopathy. Both patients had acanthocytosis, elevated creatine kinase (CK), and absence of chorein on Western blot analysis. The presence of chorea and neuropsychiatric disturbances associated with elevated CK levels, epilepsy, hyporeflexia, and acanthocytosis suggests the diagnosis of ChAc. Chorein assay of peripheral blood confirms the diagnosis. (c) 2008 Movement Disorder Society.
LanguageENG
Pub Type(s)JOURNAL ARTICLE
PubMed ID18785241
  
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