Management of Prader-Labhart-Willi syndrome in children and in adults, with particular emphasis on the treatment with recombinant human growth hormone

INTRODUCTION: Prader-Willi syndrome (PWS) is a genetically determined disease that manifests itself in a number of abnormalities resulting, among others, from dysfunction of the hypothalamic-pituitary system. Only integrated, multidisciplinary care gives patients the chance to significantly improve...

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Detalles Bibliográficos
Autores principales: Drabik, Marta, Lewiński, Andrzej, Stawerska, Renata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2022
Materias:
Review paper | Praca poglądowa
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226360/
https://www.ncbi.nlm.nih.gov/pubmed/35307998
http://dx.doi.org/10.5114/pedm.2022.112861

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226360/
https://www.ncbi.nlm.nih.gov/pubmed/35307998
http://dx.doi.org/10.5114/pedm.2022.112861

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