Molecular Pathogenesis of Kallmann’s Syndrome

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 β-subunits, or various transcription factors involved in pituitary g...

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Veröffentlicht in:	Hormone research 2007-01, Vol.67 (5), p.231-242
Hauptverfasser:	Cadman, Steven Mark, Kim, Soo-Hyun, Hu, Youli, González-Martínez, David, Bouloux, Pierre-Marc
Format:	Artikel
Sprache:	eng
Schlagworte:	Extracellular Matrix Proteins - genetics Extracellular Matrix Proteins - physiology Genes, Dominant Genes, X-Linked Gonadotropin-Releasing Hormone - genetics Gonadotropin-Releasing Hormone - metabolism Gonadotropin-Releasing Hormone - physiology Heparan Sulfate Proteoglycans - physiology Humans Kallmann Syndrome - etiology Kallmann Syndrome - genetics Mini Review Models, Biological Nerve Tissue Proteins - genetics Nerve Tissue Proteins - physiology Olfactory Bulb - embryology Olfactory Bulb - metabolism Receptor, Fibroblast Growth Factor, Type 1 - genetics Receptor, Fibroblast Growth Factor, Type 1 - physiology Receptors, LHRH - genetics Receptors, LHRH - metabolism Receptors, LHRH - physiology Signal Transduction
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