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Article

Molecular Pathogenesis of Kallmann’s Syndrome

21 Dec 2006

Abstract excerpt

Hypogonadotrophic hypogonadism (HH) is characterized by delayed or absent pubertal development secondary to gonadotrophin deficiency. HH can result from mutations of the gonadotrophin-releasing hormone receptor 1, the gonadotrophin beta-subunits, or various transcription factors involved in pituitary gland development. HH occurs in DAX1 mutations when associated with adrenal insufficiency (adrenal hypoplasia...

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Identifiers

PMID: 17191030
DOI: 10.1159/000098156

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