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 (Author), Espelid Ivar (Author), Storhaug Kari (Author), Sandvik Leiv (Author), Nordgarden Hilde (Author)
Format: Book
Published: BMC, 2012-05-01T00:00:00Z.
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