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Article

Congenital hypogonadotropic hypogonadism in females: clinical spectrum, evaluation and genetics.

Annales d'endocrinologie - 1 May 2010

Bry-Gauillard H, Trabado S, Bouligand J, Sarfati J, Francou B, Salenave S, Chanson P, Brailly-Tabard S, Guiochon-Mantel A, Young J

Abstract excerpt

Congenital hypogonadotropic hypogonadisms (CHH) are a well-known cause of pubertal development failure in women. In a majority of patients, the clinical spectrum results from an insufficient and concomitant secretion of both pituitary gonadotropins LH and FSH that impedes a normal endocrine and exocrine cyclical ovary functioning after the age of pubertal activation of gonadotropic axis. In exceptional but...

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Source

Identifiers

PMID: 20363464
DOI: 10.1016/j.ando.2010.02.024

Genes

CHD7
FGF8
FGFR1
PROK2
PROKR2
TAC3
TACR3

Provenance

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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Congenital hypogonadotropic hypogonadism in females: clinical spectrum, evaluation and genetics.PMID 20363464Read ↗

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Genetic and phenotypic differences between sexes in congenital hypogonadotropic hypogonadism (CHH): Large cohort analysis from a single tertiary centre.Semantic proximity Read ↗

Congenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: Past, Present, and FutureSemantic proximity Read ↗

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