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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Detalles Bibliográficos
Autores principales: Yanagita, Manabu, Hirano, Hiroyuki, Kobashi, Mariko, Nozaki, Takenori, Yamada, Satoru, Kitamura, Masahiro, Murakami, Shinya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3159111/
https://www.ncbi.nlm.nih.gov/pubmed/21798057
http://dx.doi.org/10.1186/1752-1947-5-329

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3159111/
https://www.ncbi.nlm.nih.gov/pubmed/21798057
http://dx.doi.org/10.1186/1752-1947-5-329

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