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Wiedzieć więcej o zespole Pradera–Williego. Opieka wielospecjalistyczna  151–166 To know more about the Prader–Willi syndrome. Multidisciplinary support  151–166
 
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Psychiatr Pol 2009;43(2):151-166
 
SŁOWA KLUCZOWE
STRESZCZENIE
Prader-Willi syndrome, induced by a loss of function of paternal genes in the subcentrometric region of the chromosome 15 (q11.2q13), is a complex neurodevelopmental disorder with characteristic obesity resulting from hyperphagia. In addition behavioural disturbancies with obsessive-compulsive features, aggression, temper tantrums included, are relatively frequently seen and they often require psychiatric intervention. In this part of the paper we reviewed the recent data of behavioural phenotype the correlations of phenotype-genotype and possibilities of the multidisciplinary support for the affected persons and theirs families.
eISSN:2391-5854
ISSN:0033-2674
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