The oro-dental phenotype in Prader–Willi syndrome: a survey of 15 patients

Prader–Willi syndrome (PWS) is a complex disorder characterized by severe neonatal hypotonia and feeding problems, childhood-onset hyperphagia and obesity, short stature, facial dysmorphy, hypogonadism, and learning and behavioural difficulties 1 . It is a rare disorder caus...

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Main Author: ISABELLE BAILLEUL-FORESTIER
Format: Koleksi Audio Visual
Language: Bahasa Inggris
Published: IAPD and Blackwell 2008
Subjects:
Online Access: http://oaipmh-jogjalib.umy.ac.idkatalog.php?opo=lihatDetilKatalog&id=94118
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