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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2012-05-01
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Series: | BMC Oral Health |
Subjects: | |
Online Access: | http://www.biomedcentral.com/1472-6831/12/12 |