【摘要】 Kallm ann综合征是一种罕见的遗传病,它表现为促性腺激素分泌不足的性腺功能减退伴嗅觉丧失或嗅觉减退。目前研究已发现Kallm ann综合征的3种遗传方式及其相关的疾病基因。现对Kallm ann综合征的临床诊治及疾病基因的研究进展作一综述。更多还原

【Abstract】 Kallmann syndrome(KS) is a rare hereditary disease.It is characterized by hypogonadotrophic hyponadism 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.更多还原