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Wiedzieć więcej o zespole Pradera–Williego. Diagnostyka  135–149 To know more about the Prader–Willi syndrome. Diagnosis  135–149
 
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Psychiatr Pol 2009;43(2):135-149
 
SŁOWA KLUCZOWE
STRESZCZENIE
Prader-Willi syndrome, induced by a function changes of paternal genes in the subcentrometric region of the chromosome 15 (q11.2q13), is the most common genetic cause of obesity resulting from hyperphagia. Behavioural disturbancies with compulsions in which psychiatric interventions are necessary, are relatively frequently seen. In this paper we reviewed the recent data of the clinical diagnosis verified by molecular studies.
eISSN:2391-5854
ISSN:0033-2674
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