Adult-onset reversible idiopathic hypogonadotropic hypogonadism in male adult carrying a WDR11 missense mutation

Idiopathic hypogonadotropic hypogonadism (IHH) occurs mostly in childhood or adolescence and very rarely in adulthood. It is characterised by delayed onset of secondary sexual characteristics. Many genetic abnormalities have been reported in congenital IHH cases, but rarely in adult-onset IHH cases....

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Detalles Bibliográficos
Autores principales: Yamada, Rie, Yamakita, Noriyoshi, Yasuda, Keigo, Imai, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Case Reports: Reminder of important clinical lesson
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494561/
https://www.ncbi.nlm.nih.gov/pubmed/36130823
http://dx.doi.org/10.1136/bcr-2022-250444

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494561/
https://www.ncbi.nlm.nih.gov/pubmed/36130823
http://dx.doi.org/10.1136/bcr-2022-250444

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