Progression of genetic study in idiopathic hypogonadotropic hypogonadism
10.3760/cma.j.issn.1000-6699.2012.03.022
- VernacularTitle:特发性低促性腺激素性性腺功能减退症的遗传学研究进展
- Author:
Ruya LIU
;
Xiaoying LI
- Publication Type:Journal Article
- Keywords:
Idiopathic hypogonadotropic hypogonadism;
Genetics
- From:
Chinese Journal of Endocrinology and Metabolism
2012;28(3):244-248
- CountryChina
- Language:Chinese
-
Abstract:
Idiopathic hypogonadotropic hypogonadism(IHH) is a complex oligogenic disease.About 60％ of patients are associated with anosmia or hyposmia,also known as Kallmann syndrome. Based on genetic and molecular biological research,about more than ten IHH responsible genes have been discovered.
