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1996年至今,我院共收治男性假两性畸形9例,其中假阴道型尿道下裂综合征6例,睾丸女性化综合征3例。临床资料 6例假阴道型尿道下裂综合征除1例2岁患儿未确定社会性别外,其余5例年龄19～27岁;3例社会性别为男性,2例为女性;汉族4人,维吾尔族2人。6例病人的共同临床特点是无家族遗传史。查体:身高168～185cm,体重60～75kg,男性体态和男性脂肪分布,手脚粗大,有喉结,语音粗沉和腋毛稀少,阴毛呈倒三角形(以上体检特点除外2岁患儿),乳
Since 1996, our hospital treated 9 cases of male pseudohermaphroditism, including 6 cases of false vaginal hypospadias syndrome and 3 cases of testicular feminization syndrome. Clinical data 6 cases of fake vaginal hypospadias syndrome in 1 case of 2-year-old children did not determine the gender, the remaining 5 cases aged 19 to 27 years; 3 cases of male gender, 2 cases of female; Han 4, Uyghur Family 2 people. The common clinical features of 6 patients were family history. Physical examination: height 168 ~ 185cm, weight 60 ~ 75kg, male body and fat distribution, hands and feet thick, Adam’s apple, voice coarse and thin armpit hair, pubic hair was inverted triangle (except the above physical examination characteristics of 2-year-old children)