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

BACKGROUND: 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 dysmorphology and oral abnormalities. The purpose of the present...

Descripción completa

Detalles Bibliográficos
Autores principales: Saeves, Ronnaug, Espelid, Ivar, Storhaug, Kari, Sandvik, Leiv, Nordgarden, Hilde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437195/
https://www.ncbi.nlm.nih.gov/pubmed/22639910
http://dx.doi.org/10.1186/1472-6831-12-12

Ejemplares similares

Ejemplares similares