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Periodontal disease in a patient with Prader-Willi syndrome: a case report
INTRODUCTION: Prader-Willi syndrome is a complex genetic disease caused by lack of expression of paternally inherited genes on chromosome 15q11-q13. The prevalence of Prader-Willi syndrome is estimated to be one in 10,000 to 25,000. However, descriptions of the oral and dental phenotype are rare. CA...
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| 主要な著者: | , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2011
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3159111/ https://ncbi.nlm.nih.gov/pubmed/21798057 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-5-329 |
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