真两性畸形为两性畸形中比较少见的类型。我院于1983年12月收治一例,现报告如下。病例:2岁,社会性别男,住院号87252。患儿出生后其父母亲发现患儿尿道口位置异常,阴茎弯曲,排尿未见异常。患儿系足月妊娠第一胎,顺产。父母亲分娩年龄分别为25、23岁。否认怀孕期间患疾病史、服药史以及与有害物质接触史,其母亲无自然流产史。父母亲非近亲婚配。体查:精神较差,未见特殊面容,不会行走,头围46.7cm,胸围47.1cm,前囱未闭,体重11kg,身高80cm,阴茎下层畸形Ⅰ级,阴茎头扁平,背侧包皮稍长,尿道开口于阴囊后部,未见其他开口,左侧阴囊呈大阴唇样,未 True hermaphroditism is a relatively rare type of hermaphroditism. Our hospital in December 1983 admitted a case, the report is as follows. Case: 2 years old, male gender, hospital number 87252. Children born after their parents found abnormal urethral orifice position, penile curvature, no abnormal urination. Children with first-term full-term pregnancy, spontaneous delivery. Parental delivery age were 25,23 years old. Denied the history of illness during pregnancy, medication history and history of contact with harmful substances, the mother had no history of spontaneous abortion. Parents are not close relatives. Physical examination: poor spirit, no special face, no walking, head circumference 46.7cm, chest circumference 47.1cm, anterior chimney, weight 11kg, height 80cm, lower deformity level Ⅰ penis, flat head, dorsal foreskin slightly Long, urethral opening in the back of the scrotum, no other openings, the left scrotum was labia majora-like, not