Severe tooth wear in Prader-Willi syndrome. A case–control study

<p>Abstract</p> <p>Background</p> <p>Prader-Willi syndrome (PWS) is a rare complex multsystemic genetic disorder characterized by severe neonatal hypotonia, endocrine disturbances, hyperphagia and obesity, mild mental retardation, learning disabilities, facial dysmorpho...

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Bibliographic Details
Main Authors: Saeves Ronnaug, Espelid Ivar, Storhaug Kari, Sandvik Leiv, Nordgarden Hilde
Format: Article
Language:English
Published: BMC 2012-05-01
Series:BMC Oral Health
Subjects:
Online Access:http://www.biomedcentral.com/1472-6831/12/12