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Kallmann综合征(KS)又称为性幼稚嗅觉丧失综合征,其特征是选择性促性腺功能低下型性腺功能减退和嗅觉缺失,是一种少见的先天性疾病。早期发现并给予激素替代治疗可使该病患者恢复性腺功能。现将1998年至今我们诊治的12例Ksllmann综合征报告如下。1临床资料本组12例均为男性,年龄19-28岁,主诉为第二性征及外生殖器发育不良伴嗅觉缺失7例,以因婚后不育就医5例。追同病史12例患者均自幼发现外生殖器较同龄人小,青春期后外生殖器男性第二性征不发育(如男性无胡须及阴
Kallmann’s syndrome (KS), also known as sexual immature olfactory loss syndrome, is characterized by a combination of hypogonadal hypogonadism and loss of sense of smell, a rare congenital condition. Early detection and hormone replacement therapy can restore the patient’s gonadal function. Now from 1998 to now we diagnosed 12 cases of Ksllmann syndrome are reported below. 1 Clinical data The group of 12 patients were male, aged 19-28 years old, the main complaint of secondary sexual characteristics and genital malformations with loss of smell in 7 cases, because of infertility treatment in 5 cases. In the 12 years following the medical history, the genitalia were found to be younger than their peers and the second sexual characteristics of male genitalia were undeveloped after adolescence (eg, male with no beard and yin