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[Advances in the studies of Kallmann syndrome].

作者信息

Hao Li-jun, Cui Ying-xia

机构信息

Laboratory of Reproduction and Genetics, Nanjing General Hospital, Nanjing command, PLA, Nanjing, Jiangsu 210002, China.

出版信息

Zhonghua Nan Ke Xue. 2006 Jul;12(7):647-9.

Abstract

Kallmann syndrome (KS) is a rare hereditary disease. It is characterized by hypogonadotrophic hypogonadism in association with anosmia or hyposmia. At present, three modes of inheritance and genes related to KS have been identified. This review focuses on the clinical diagnosis and advances in the studies of the pathogenesis gene for Kallmann syndrome.

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