Oral disorders in children with Prader-Willi syndrome: a case control study | Orphanet Journal of Rare Diseases | Full Text

Oral disorders in children with Prader-Willi syndrome: a case control study | Orphanet Journal of Rare Diseases | Full Text

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

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 abnormali...

Authors:Carla Munné-Miralvés, Lluís Brunet-Llobet, Abel Cahuana-Cárdenas, Sergi Torné-Durán, Jaume Miranda-Rius and Alejandro Rivera-Baró

Citation:Orphanet Journal of Rare Diseases 2020 15:43

Content type:Research

Published on: 10 February 2020

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