Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland

Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland

<p>Abstract</p> <p>Background</p> <p>Kallmann syndrome (KS), comprised of congenital hypogonadotropic hypogonadism (HH) and anosmia, is a clinically and genetically heterogeneous disorder. Its exact incidence is currently unknown, and a mutation in one of the identified...

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Bibliographic Details
Main Authors: Tommiska Johanna, Vaaralahti Kirsi, Laitinen Eeva-Maria, Eklund Elina, Tervaniemi Mari, Valanne Leena, Raivio Taneli
Format: Article
Language:English
Published: BMC 2011-06-01
Series:Orphanet Journal of Rare Diseases
Online Access:http://www.ojrd.com/content/6/1/41

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http://www.ojrd.com/content/6/1/41

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