Treatment of congenital hypogonadotropic hypogonadism in male patients

Congenital hypogonadotropic hypogonadism (CHH) is characterized by complete or partial failure of pubertal development because of inadequate secretion of gonadotropic hormones. CHH consists of hypogonadotropic hypogonadism with anosmia or hyposmia, Kallmann syndrome, and the normosmic variation norm...

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Detalles Bibliográficos
Autores principales: Lee, Hae Sang, Shim, Young Suk, Hwang, Jin Soon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Pediatric Endocrinology 2022
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537667/
https://www.ncbi.nlm.nih.gov/pubmed/36203268
http://dx.doi.org/10.6065/apem.2244208.104

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537667/
https://www.ncbi.nlm.nih.gov/pubmed/36203268
http://dx.doi.org/10.6065/apem.2244208.104

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