Advances in the studies of Kallmann syndrome.
- Author:
Li-jun HAO
1
;
Ying-xia CUI
Author Information
1. Laboratory of Reproduction and Genetics, Nanjing General Hospital, Nanjing command, PLA, Nanjing, Jiangsu 210002, China.
- Publication Type:Journal Article
- MeSH:
Diagnosis, Differential;
Extracellular Matrix Proteins;
genetics;
Humans;
Kallmann Syndrome;
diagnosis;
genetics;
therapy;
Male;
Nerve Tissue Proteins;
genetics;
Rare Diseases;
Receptor, Fibroblast Growth Factor, Type 1;
genetics
- From:
National Journal of Andrology
2006;12(7):647-649
- CountryChina
- Language:Chinese
-
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.
