Idiopathic central precocious puberty with Prader–Willi syndrome: pubertal development with discontinuation of gonadotropin-releasing hormone analog

SUMMARY: Prader–Willi syndrome (PWS) is a genetic imprinting disorder that is characterized by obesity, short stature, and hypogonadism. Hypogonadism is characterized by normal luteinizing hormone (LH), high follicle-stimulating hormone (FSH), low testosterone, low inhibin B, and relatively low anti...

Descripción completa

Detalles Bibliográficos
Autores principales: Kobayashi, Mami, Yagasaki, Hideaki, Tamaru, Kei, Mitsui, Yumiko, Inukai, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2022
Materias:
Unique/Unexpected Symptoms or Presentations of a Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9422229/
https://www.ncbi.nlm.nih.gov/pubmed/36017812
http://dx.doi.org/10.1530/EDM-22-0244

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9422229/
https://www.ncbi.nlm.nih.gov/pubmed/36017812
http://dx.doi.org/10.1530/EDM-22-0244

Ejemplares similares