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Article

Diagnosis and treatment analysis of a case of idiopathic hypogonadotropic hypogonadism caused by NSMF gene mutation.

Yi chuan = Hereditas - 1 May 2026

Peng Shu-Yi, Wang Kai, Wang Shu-Qi, Zhang Ming-Jin, Sheng Pei, An Xiao-Fei

Abstract excerpt

Idiopathic hypogonadotropic hypogonadism (IHH) is a rare endocrine disorder characterized by deficiency or dysfunction of endogenous gonadotropin-releasing hormone (GnRH), leading primarily to hypogonadism. Based on the presence or absence of olfactory dysfunction, IHH is classified into Kallmann syndrome (KS) and normosmic IHH (nIHH). In this study, we reported a 15-year-old male with nIHH, presenting with...

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Identifiers

PMID: 42145198
DOI: 10.16288/j.yczz.25-187

Genes

IHH
NSMF

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Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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