Clinical, hormonal, and genetic characteristics of 25 Chinese patients with idiopathic hypogonadotropic hypogonadism

BACKGROUND: Idiopathic hypogonadotropic hypogonadism (IHH) is a type of congenital disease caused by a variety of gene variants leading to dysfunction in the secretion of hypothalamic gonadotropin-releasing hormones (GnRHs). Clinically, IHH can be divided into Kallmann syndrome (KS) with dysosmia an...

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Detalles Bibliográficos
Autores principales: Liu, Qingxu, Yin, Xiaoqin, Li, Pin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8796337/
https://www.ncbi.nlm.nih.gov/pubmed/35090434
http://dx.doi.org/10.1186/s12902-022-00940-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8796337/
https://www.ncbi.nlm.nih.gov/pubmed/35090434
http://dx.doi.org/10.1186/s12902-022-00940-9

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