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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...

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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

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