Oral disorders in children with Prader-Willi syndrome: a case control study

INTRODUCTION: Prader-Willi Syndrome (PWS) is a genetic disorder caused by the lack of expression of certain paternal genes located on chromosome 15q11-q13. This anomaly causes cognitive, neurological and endocrine abnormalities, among which one of the most important is hyperphagia. The aim of this s...

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Detalles Bibliográficos
Autores principales: Munné-Miralvés, Carla, Brunet-Llobet, Lluís, Cahuana-Cárdenas, Abel, Torné-Durán, Sergi, Miranda-Rius, Jaume, Rivera-Baró, Alejandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011482/
https://www.ncbi.nlm.nih.gov/pubmed/32041633
http://dx.doi.org/10.1186/s13023-020-1326-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011482/
https://www.ncbi.nlm.nih.gov/pubmed/32041633
http://dx.doi.org/10.1186/s13023-020-1326-8

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