Normosmic idiopathic hypogonadotropic hypogonadism (IHH) and Kallmann syndrome are rare congenital forms of secondary hypogonadism characterized by delayed or absent sexual development.

This is an international collaboration assembling the largest cohort of CHH reversals to date. We are applying latent class mixture modeling to identify predictors of reversal and relapse. 1) we ...

Previous research had revealed that mutations in genes associated with TACR3 led to a condition known as “congenital hypogonadism,” resulting in lower production of sex hormones, including ...

Hummel and colleagues (1) we would like to mention a recent review on the topic of genetic causes of congenital hypogonadism which describes in detail how dysfunction in the sense of smell is ...

Elderly. Nursing mothers: not recommended. Testosterone replacement therapy in adult males with congenital or acquired primary hypogonadism or hypogonadotropic hypogonadism. To stimulate puberty ...