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

Primary hypogonadism (hypergonadotropic hypogonadism) occurs when the hormone deficiency is due to problems in the sex glands, or gonads—the female ovaries and male testes.

Recognition, Management, and Action,” published in the December 2024 issue of Endocrinology by McDermott. Pseudo-endocrine ...

Its growth is driven by a rising awareness of hypogonadism. The global testosterone replacement therapy (TRT) market is projected to grow by $461m by 2029 at a compound annual growth rate of 3.3%, ...