Prader-Willi Syndrome and psychotic symptoms: 1. Case descriptions and genetic studies

By: Clarke, D (et al).
Series: Journal of Intellectual Disability Research 46 (2) 2002: 451-454. 2002Content type: text Media type: unmediated Carrier type: volume Subject(s): CASE STUDIES | DUAL DIAGNOSIS | GENETICS | PRADER WILLI SYNDROMESummary: Genetic studies were possible in five cases and SNRPN expression was examined in three cases. Maternal unipartental disomy and 15q11q13 deletions were found, demonstrating that pyschotic symptoms are not associated with a single type of genetic abnormality. [AJ]
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Genetic studies were possible in five cases and SNRPN expression was examined in three cases. Maternal unipartental disomy and 15q11q13 deletions were found, demonstrating that pyschotic symptoms are not associated with a single type of genetic abnormality. [AJ]

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