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

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

Publikováno v: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)

Abstract 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 o

Externí odkaz: https://doaj.org/article/e4a4ac76efc8498a8ee90c78da8a8ab4

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

Autor: Munné-Miralvés C, Brunet Ll, Abel Belizario Cahuana Cardenas, Torné-Durán S, Miranda-Rius J, Rivera-Baró A

Publikováno v: ORPHANET JOURNAL OF RARE DISEASES
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu

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 th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::46cef8cf935db3b7904c96d34ca1342c
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=17397