女性假两性畸形

Of the 14 patients, 5 were true hermaphroditism, 5 female pseudohermaphroditism and 4 male pseudohermaphroditism.

本文报道了14例两性畸形，其中真两性畸形5例，女性假两性畸形5例，男性假两性畸形4例。

Fig 3 Male pseudohermaphrodite raised as a female,Preopera-tive and 7 days postoperatively

图3抚养为女性的男性假两性畸形，术前和术后7d

Methods The CT findings in 4 cases of female pseudohermaphroditism were analyzed retrospectively.

回顾性分析4例经手术及临床诊断为女性假两性畸形的CT表现。

Objective To evaluate the CT findings of female pseudohermaphroditism.

目的 评价女性假两性畸形的CT表现特点及其临床价值。

Objective To evaluate the CT findings of female pseudohermaphroditism. Methods The CT findings in 4 cases of female pseudohermaphroditism were analyzed retrospectively.

目的 评价女性假两性畸形的CT表现特点及其临床价值方法回顾性分析4例经手术及临床诊断女性假两性畸形的CT表现。

Female pseudohermaphroditism is a genetic disease ,early detection and early treatment are very importment.

女性假两性畸形是遗传性疾病，早期诊断和早期治疗极其重要。

Male pseudohermaphroditism has been well-described in the testicular feminizing syndrome of man.

雄性的假两性畸形在男性睾丸女性化的综合症中已有报道。

Objective To evaluate the diagnosis and treatment of female pseudohermaphroditism caused by 21-hydroxylase deficiency.

目的 探讨21-羟化酶缺乏（21-hydroxylase deficiency，21-OHD）致女性假两性畸形的临床诊断及治疗方法。

Five fetuses were diagnosed with female pseudohermaphroditism (21-hydroxylase deficiency in 3 and urorectal septum malformation sequence in 2). Four fetuses were diagnosed with male pseudohermaphroditism (1 with steroid sulfatase deficiency, 1 with presumed camptomelic dysplasia, and 2 undetermined).

在这16个胎儿中有5个被诊断为女性假两性畸形（其中3个有21-羟化酶分泌不足，2个有尿道直肠隔畸形），4个被诊断为男性假两性畸形（其中1个有类固醇硫酸酯酶分泌不足，1个推测可能为弯肢性发育异常，另外2个原因未定），5个有染色体异常，2个有性逆转，核型为（46，XX+SRY）。

Objective To investigate the effects of interleukin-1 β converting enzyme gene on the biologic characteristics of ovarian cancer cells.

目的 探讨白细胞介素-1 β转换酶的表达，对卵巢癌细胞生物学特性的影响。

Campylobacter: This illness is the most commonly identified cause of diarrheal illness in the world.

弯曲：这种病是最常见的原因查明腹泻病，在世界上。