Clinical and molecular features of 40 Chinese patients with idiopathic hypogonadotropic hypogonadism

BACKGROUND: Male idiopathic hypogonadotropic hypogonadism (IHH) is a heterogeneous clinical rare genetic disorder that can be divided into two forms: Kallmann syndrome (KS) and olfactory normal IHH (nIHH). Nearly half of unknown pathogenic genes and related pathogenic mechanisms have yet to be explo...

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Detalles Bibliográficos
Autores principales: Wang, Yuanfan, Jiang, Weijun, Xia, Xinyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560348/
https://www.ncbi.nlm.nih.gov/pubmed/37814704
http://dx.doi.org/10.21037/tau-23-225

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560348/
https://www.ncbi.nlm.nih.gov/pubmed/37814704
http://dx.doi.org/10.21037/tau-23-225

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