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

BACKGROUND: 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 KS genes has only been found in ~30% of the patients....

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Detalles Bibliográficos
Autores principales: Laitinen, Eeva-Maria, Vaaralahti, Kirsi, Tommiska, Johanna, Eklund, Elina, Tervaniemi, Mari, Valanne, Leena, Raivio, Taneli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143089/
https://www.ncbi.nlm.nih.gov/pubmed/21682876
http://dx.doi.org/10.1186/1750-1172-6-41

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143089/
https://www.ncbi.nlm.nih.gov/pubmed/21682876
http://dx.doi.org/10.1186/1750-1172-6-41

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