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kallman氏综合征是一种罕见病。我院生殖内分泌门诊近年发现同一家族2例,现报道如下: 例1,男,23岁。因婚后2年不育来院求治。患者系第5胎足月顺产,母孕期正常。学习成绩较差。父母非近亲。兄、姐各2人发育正常,均已结婚并有生育。一妹系原发性闭经(见例2)。患者生殖器官一直未发育,无男性第二性征,性欲低下,无射精或遗精。体查:血压16/10.7kpa,
Kallman’s syndrome is a rare disease. Reproductive and endocrine clinic in our hospital found two cases of the same family in recent years, are reported as follows: Example 1, male, 23 years old. 2 years after marriage to seek treatment for infertility. The patient is the fifth full-term fetus, normal pregnancy during pregnancy. Poor academic performance. Parents are not close relatives. Brother and sister each 2 normal development, have been married and have fertility. A sister Department of primary amenorrhea (see Example 2). The patient’s reproductive organs have not been developed, no secondary sexual characteristics, low sexual desire, no ejaculation or nocturnal emission. Physical examination: blood pressure 16 / 10.7kpa,