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Article

Treatment of congenital hypogonadotropic hypogonadism in male patients

29 Sept 2022

Abstract excerpt

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 normosmic idiopathic hypogonadotropic hypogonadism. CHH is one of the few treatable diseases of male infertility,...

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Share to Hormonal and reproductive studies
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PMID: 36203268
DOI: 10.6065/apem.2244208.104

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