Kallmann syndrome and hypogonadotropic hypogonadism
Kallmann syndrome and hypogonadotropic hypogonadism:

Over the past decade, the understanding of the processes involved in the regulation of gonadotropin-releasing hormone and its dysfunction has greatly increased. As new regulatory peptides have been identified, the underlying causes of central hypogonadism have multiplied, and the area has become inc...

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Bibliographic Details
Other Authors: Quinton, Richard (Editor)
Format: Electronic eBook
Language:English
Published: Basel Karger 2010
Series:Frontiers of hormone research Vol. 39
Subjects:
Hypogonadism
Hypogonadism > genetics
Kallmann Syndrome > genetics
Molekulargenetik
Hypogonadotroper Hypogonadismus
Online Access:DE-522
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Summary:Over the past decade, the understanding of the processes involved in the regulation of gonadotropin-releasing hormone and its dysfunction has greatly increased. As new regulatory peptides have been identified, the underlying causes of central hypogonadism have multiplied, and the area has become increasingly complex. The reversibility of even genetically determined hypogonadotropic hypogonadism has become more firmly established, and clinical studies have greatly expanded our understanding of basic physiological pathways. Structuring this mass of new knowledge in thirteen comprehensive chapters, a group of renowned experts, representing the principal international research groups, take stock of the most recent progress.This up-to-date overview helps scientists and clinicians to plan future research and treat patients with delayed puberty, hypogonadotropic hypogonadism and other forms of central reproductive disorders
Item Description:Genetics, developmental biology and clinical phenotypes
Physical Description:1 Online-Ressource (X, 174 Seiten) Illustrationen, Diagramme
ISBN:9783805586184
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