Psychotic disorder in a case with Hallervorden-Spatz disease
ACTA PSYCHIATRICA SCANDINAVICA, vol.108, no.5, pp.394-397, 2003 (SCI-Expanded, SSCI, Scopus)
- Publication Type: Article / Article
- Volume: 108 Issue: 5
- Publication Date: 2003
- Doi Number: 10.1034/j.1600-0447.2003.00159.x
- Journal Name: ACTA PSYCHIATRICA SCANDINAVICA
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Social Sciences Citation Index (SSCI), Scopus
- Page Numbers: pp.394-397
- Keywords: Hallervorden-Spatz disease, basal ganglia, psychotic disorder
- Ankara University Affiliated: No
Abstract
Objective: Hallervorden - Spatz disease is a rare autosomal recessive condition, with early onset of predominantly extrapyramidal dysfunction. The symptoms of the disease are dystonia, rigidity, choreoathetosis, pyramidal signs, and intellectual decline. Recent genetic studies mapped the disease to chromosome 20p12.3-p13, and identified mutations in the pantothenate kinase gene. This report describes a childhood onset case of Hallervorden - Spatz disease with schizophreniform psychotic symptoms. Former reports about the psychiatric comorbidity generally included depressive disorder.