论文部分内容阅读
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。
Kallm ann syndrome is a rare genetic disease characterized by hypogonadotropic hypogonadism with loss of olfactory or loss of smell. The current study has found three genetic Kallm ann syndrome and its associated disease genes. Now Kallm ann syndrome clinical diagnosis and treatment of disease genes are reviewed.