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男性,34岁。27岁时因其无生育能力,与妻子离婚受刺激而发病,以分裂症样症状曾先后住院4次,疾病间歇期精神活动基本正常。伯父有性发育不全史。体检:20岁时身高176cm、体重70kg,34岁时身高增高到192cm、体重达90.5kg。先天性嗅觉丧失。手指细长.指距20cm。青春期后第二性征发育不良,阴茎似幼童型.无阴毛腋毛,无胡须,喉结,皮肤细腻,面色红润似女人面容,言调细尖,睾丸小。实验室检查:尿moncs17.2/24h、尿17—ks3.8mg/24h;血HCG(-)、HBcAgl: 32(+);精液量少为0.5ml,无精子。
Male, 34 years old. 27-year-old due to their non-fertility, divorced by his wife stimulated the onset of schizophrenia-like symptoms have been hospitalized 4 times, intermittent mental illness was normal. Uncle history of sexual dysplasia. Physical examination: height 20cm height 176cm, weight 70kg, 34-year-old height increased to 192cm, weighing 90.5kg. Congenital loss of smell. Finger slender. Finger pitch 20cm. Secondary sexual characteristics after puberty dysplasia, penis-like child-like type. No pubic hair armpit hair, no beard, Adam’s apple, delicate skin, ruddy like a woman’s face, slender speech, testicular small. Laboratory tests: urine moncs17.2 / 24h, urine 17-ks3.8mg / 24h; blood HCG (-), HBcAgl: 32 (+); semen less 0.5ml, no sperm.