GNRHR-related central hypogonadism with spontaneous recovery – case report

BACKGROUND: Congenital hypogonadotropic hypogonadism (CHH) is a clinically and genetically heterogeneous disease characterized by absent or incomplete puberty and infertility. Clinical characteristics are secondary to insufficient gonadotropin secretion, caused by deficient gonadotropin-releasing ho...

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Detalles Bibliográficos
Autores principales: Šmigoc Schweiger, Darja, Davidović Povše, Maja, Trebušak Podkrajšek, Katarina, Battelino, Tadej, Avbelj Stefanija, Magdalena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652797/
https://www.ncbi.nlm.nih.gov/pubmed/36371229
http://dx.doi.org/10.1186/s13052-022-01377-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652797/
https://www.ncbi.nlm.nih.gov/pubmed/36371229
http://dx.doi.org/10.1186/s13052-022-01377-5

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