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