Kallmann综合征又称促性腺激素分泌不足的性腺功能减退伴嗅球丧失症,是一种先天性的遗传病[1]。最早由Kallmann于1944年报道,男女均可发病,男性发病率约为1/10000,女性发病率约为1/50000。本科于2008年8月诊治1例Kallmann综合征患者,现报告如下。1临床资料患者,女性,15岁,因第 Kallmann syndrome, also known as hypogonadotropic hypogonadism with olfactory bulb loss, is a congenital genetic disease [1]. The earliest reported by Kallmann in 1944, both men and women can be morbidity, the incidence of males is about 1/10000, the incidence of females is about 1/50000. Undergraduate in August 2008 diagnosis and treatment of a Kallmann syndrome patients, are as follows. 1 clinical data, female, 15 years old, due to the first