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

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

Publikováno v: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)
Orphanet Journal of Rare Diseases
Dipòsit Digital de la UB
Universidad de Barcelona

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dee9662235efad67c79166a9e8562e39
https://doaj.org/article/e4a4ac76efc8498a8ee90c78da8a8ab4

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

Autor: Munné-Miralvés, Carla¹ (AUTHOR), Brunet-Llobet, Lluís^1,2 (AUTHOR) lbrunet@sjdhospitalbarcelona.org, Cahuana-Cárdenas, Abel¹ (AUTHOR), Torné-Durán, Sergi³ (AUTHOR), Miranda-Rius, Jaume^1,2,3 (AUTHOR), Rivera-Baró, Alejandro^1,2 (AUTHOR)

Publikováno v: Orphanet Journal of Rare Diseases. 2/10/2020, Vol. 15 Issue 1, p1-7. 7p.