Your browser doesn't support javascript.
loading
Sequelae of GH Treatment in Children with PWS.
Tauber, Maïthé; Diene, Gwenaelle; Molinas, Catherine.
  • Tauber M; Centre de référence du syndrome de Prader-Willi, Hôpital des Enfants, CHU Toulouse, France, Axe Pédiatrique du CIC 9302/INSERM. Hôpital des Enfants, Toulouse, France, Centre de Physiopathologie de Toulouse-Purpan, Université de Toulouse, CNRS UMR 5282, INSERM UMR 1043, Université Paul Sabatier, Toulouse, France.
  • Diene G; Centre de référence du syndrome de Prader-Willi, Hôpital des Enfants, CHU Toulouse, France, INSERM UMR 1027-Université, Toulouse III Hôpital Paule de Viguier, Toulouse, France.
  • Molinas C; Centre de référence du syndrome de Prader-Willi, Hôpital des Enfants, CHU Toulouse, France, Axe Pédiatrique du CIC 9302/INSERM. Hôpital des Enfants, Toulouse, France, Centre de Physiopathologie de Toulouse-Purpan, Université de Toulouse, CNRS UMR 5282, INSERM UMR 1043, Université Paul Sabatier, Toulouse, France.
Pediatr Endocrinol Rev ; 14(2): 138-146, 2016 Dec.
Article en En | MEDLINE | ID: mdl-28508607
ABSTRACT
More than 15 years after rGH was granted marketing authorization for children with PWS, a review of the sequelae, side effects and safety issues of rGH therapy is timely. The publications on issues concerning respiratory function, glucose metabolism, fat mass, and scoliosis at baseline and with rGH treatment are herein presented. We discuss the impact of rGH side effects, make proposals to prevent or treat them, and emphasise the remaining questions and perspectives. As a whole, the benefit /risk ratio is positive, although questions are raised about the role of GH in premature pubarche and its long-term effects, particularly the potential long-term oncogenic risk. The organisation of care in dedicated or reference centres at the national and European level will facilitate the collection and analysis of data and serve as a paradigm for long-term follow-up.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / Hormona de Crecimiento Humana Límite: Child / Humans Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / Hormona de Crecimiento Humana Límite: Child / Humans Idioma: En Año: 2016 Tipo del documento: Article