A Clinical Experience of Pubertal Induction in Female Patients With Congenital Hypogonadotropic Hypogonadism (CHH) From an Endo-ERN Referral Center

Female congenital hypogonadotropic hypogonadism (CHH) is a rare condition, with a strong genetic background, characterized by absent or incomplete pubertal development, for which inductive treatment with sex-hormone is required. Although the available data, mostly coming from studies in patients wit...

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Vydáno v:J Endocr Soc
Hlavní autoři: Federici, Silvia, Cangiano, Biagio, Goggi, Giovanni, Persani, Luca, Bonomi, Marco
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2021
Témata:
Pediatric Endocrinology
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8090729/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvab048.1357
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