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Article

[Molecular genetics of Kallmann syndrome: an update].

Zhonghua nan ke xue = National journal of andrology - 1 Apr 2011

Fu Chao, Feng Zheng, Liu Rui-Zhi

Abstract excerpt

Kallmann syndrome (KS) is a clinically and genetically heterogeneous disorder that occurs in either an inherited or a sporadic manner. KS results from failed embryonic migration of GnRH-1 neurons from the nasal placode to the hypothalamus, due to the abnormal development of olfactory nerves and bulbs. Hypogonadotropic hypogonadism is related to GnRH deficiency, and anosmia is associated with the absence or...

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PMID: 21548217

Genes

FGF8
FGFR1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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