两性畸形是指一个个体的性器官有着男女两性的表现。可分为真两性畸形和假两性畸形。真两性畸形是指在同一个体内既有睾丸又有卵巢其外生殖器与第二性征介于两性之间。染色体核型可为正常男性型、女性型或嵌合型；假两性畸形指性腺与外生殖器不相一致，如外生殖器类似女性而内生殖器为睾丸者称男性假两性畸形，相反外生殖器类似男性，内生殖器为卵巢称为女性假两性畸形。
n. gynandrism
misc. hermaphrodism ; androgyneity ; teratismus hermaphroditicus
两性畸形人 hermaphrodite
新生儿两性畸形的处理 Newborn Ambiguous Genitalia Management
假两性畸形 spurious hermaphrodism ; false hermaphroditism ; [遗] [医] pseudohermaphroditism
嵌合型真两性畸形猪 true he aphroditic pig
男性假两性畸形 androgynism ; androgynia ; male pseudohermaphroditism
真两性畸形猪 true he aphroditic pig ; THP
双侧两性畸形 bilateral hermaphroditism ; hermaphroditismus verus bilateralis
女性假两性畸形 [妇产] female pseudohermaphroditism ; pseudarrhenia
两性畸形的 hermaphroditic
Clinical symptoms,including breast dysplasia, primary amenorrhea, bad development of secondary sexual characteristics, genital hermaphroditism, vaginal stenosis or blind side;male pseudohermaphrod- itism with gonadal dysplasia ectopic and female pseudohermaphroditism with uterine dysplasia and so on.
临床症状包括乳房发育不良、原发闭经、第二性征发育差、外阴两性畸形、阴道狭窄或呈盲端;男性假两性畸形者性腺异位及发育不良;女性假两性畸形者子宫发育不良等。
参考来源 - 假两性畸形17例病例临床分析Background17α-hydroxylase/17,20-lyase deficiency (17OHD) is a rare form of congenital adrenal hyperplasia leading to hypokalemic, hypertension and sexual abnormalities such as pseudohermaphroditism in males, and sexual infantilism in females.
17α-羟化酶/17,20碳链裂解酶缺乏症是先天性肾上腺皮质增生症中少见的类型,主要表现为低血钾、高血压及性发育障碍,在男性表现为假两性畸形或外阴女性化,而在女性则表现为第二性征发育障碍。
参考来源 - 17α·2,447,543篇论文数据，部分数据来源于NoteExpress
目的总结对真两性畸形的诊断和治疗经验。
ObjectiveTo summarize the experience of diagnosis and treatment of true hermaphroditism.
目的：总结13例真两性畸形的诊断要点及治疗体会。
Purpose: To summarize the diagnostic point and therapeutic experience of 13 cases of true hermaphroditism.
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.
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