PL EN
ARTICLE
To know more about the Prader-Willi syndrome. Diagnosis
 
More details
Hide details
 
Psychiatr Pol 2009;43(2):135-149
 
KEYWORDS
ABSTRACT
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
Journals System - logo
Scroll to top