目的为了诊断和治疗21羟化酶缺乏导致的女性假两性畸形。
Objective To diagnose and treat female pseudohermaphroditism caused by 21 - hydroxylase deficiencies.
化综合征是一种X连锁的隐性遗传病，为男性假两性畸形中最常见的类型。
Testicular feminization syndrome, the most common type of male pseudohermaphroditism, is an X-linked recessive disorder.
目的分析男性假两性畸形的临床特征，提高对男性假两性畸形的诊断和治疗水平。
Objective To improve diagnosis and treatment for male pseudohermaphroditism by analyzing their clinical characters.
其中女性假两性畸形5例。男性假两性畸形及真两性畸形各3例，社会性别均为女性。
There were 5 rases of female pseudohermaphroditism, 3 cases of male pseudohermaphroditism and true hermaphroditism in respectively.
其中女性假两性畸形5例。男性假两性畸形及真两性畸形各3例，社会性别均为女性。
There were 5 rases of female pseudohermaphroditism, 3 cases of male pseudohermaphroditism and true hermaphroditism in respectively.
应用推荐