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Congenital hypogonadotropic hypogonadism/Kallmann syndrome is associated with statural gain in both men and women: a monocentric study

Archive ouverte | Maione, Luigi | CCSD

International audience. Context Congenital hypogonadotropic hypogonadism/Kallmann syndrome (CHH/KS) is a rare condition characterized by gonadotropin deficiency and pubertal failure. Adult height (AH) in patients wi...

Similarities and differences in the reproductive phenotypes of women with congenital hypogonadotrophic hypogonadism caused by GNRHR mutations and women with polycystic ovary syndrome

Archive ouverte | Maione, Luigi | CCSD

International audience

KLB , encoding β‐Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism

Archive ouverte | Xu, Cheng | CCSD

International audience. Congenital hypogonadotropic hypogonadism (CHH) is a rare genetic form of isolated gonadotropin-releasing hormone (GnRH) deficiency caused by mutations in > 30 genes. Fibroblast growth factor ...

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