A boy with Prader-Willi syndrome: unmasking precocious puberty during growth hormone replacement therapy

Prader-Willi syndrome (PWS) is a genetic disorder frequently characterized by obesity, growth hormone deficiency, genital abnormalities, and hypogonadotropic hypogonadism. Incomplete or delayed pubertal development as well as premature adrenarche are usually found in PWS, whereas central precocious...

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Detalles Bibliográficos
Autores principales: Ludwig, Natasha G., Radaeli, Rafael F., Silva, Mariana M. X., Romero, Camila M., Carrilho, Alexandre J. F., Bessa, Danielle, Macedo, Delanie B., Oliveira, Maria L., Latronico, Ana Claudia, Mazzuco, Tânia L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Endocrinologia e Metabologia 2016
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522161/
https://www.ncbi.nlm.nih.gov/pubmed/27982202
http://dx.doi.org/10.1590/2359-3997000000196

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522161/
https://www.ncbi.nlm.nih.gov/pubmed/27982202
http://dx.doi.org/10.1590/2359-3997000000196

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