Objective To improve diagnosis and treatment for male pseudohermaphroditism by analyzing their clinical characters. 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 evaluate the imaging features of female pseudohermaphroditism. 目的评价女性假两性畸形的影像学特点。
Methods The imaging findings in9 cases of female pseudohermaphroditism were analyzed retrospectively. 方法回顾性分析9例女性假两性畸形的影像资料。
Diagnosis and Treatment of Pseudohermaphroditism 假两性畸形的诊断和治疗
Idiopathic male pseudohermaphroditism is associated with prenatal growth retardation 特发性男性假两性畸形与出生前生长发育迟缓有关
Combined treatment of female pseudohermaphroditism caused by 21-hydroxylase deficiency 21羟化酶缺乏致女性假两性畸形的治疗效果
28 cases of female pseudohermaphroditism and 22 cases of hypospadias, including 19 and 3 females. 尿道下裂22例.包括男性19例,女性3例。
Female Pseudohermaphroditism& A Report of 3 Cases 女性假两性畸形三例报告
A clinical report on the sibling with imcomplete male pseudohermaphroditism 同胞中两人患不完全性男性假两性畸形Ⅱ型的病例报告
Analysis of 26 cases of female pseudohermaphroditism 26例女性假两性畸形分析
Imaging features of female pseudohermaphroditism 女性假两性畸形影像表现
Here reported is a female pseudohermaphroditism due to 11-β-hydroxylase deficit. Its clinical forms, diagnosis and treatment were discussed. 本文报道一例先天性肾上腺皮质增生症(11&β-羟化酶缺乏)的女性患者,并对本症的临床、诊断及治疗进行了讨论。
Among the cases presented 46, XY and SRY (+), one was testicular feminization syndrome, one was XY pure gonadal dysgenesis, and six were virilizing male pseudohermaphroditism. 46,XY及SRY(+)患者中有1例为睾丸女性化综合征、1例为XY单纯性腺发育不全、6例为男性化男性假两性畸形。
Correction for female pseudohermaphroditism in 13 patients caused by extraneous androgen 药物性女性假两性畸形矫治13例分析
One-stage repair of male pseudohermaphroditism with butterfly-shaped flap from labia majora and vulva rima 带蒂皮瓣一期成形矫治男性假两性畸形
Objective To report the effect of hormone replacement plus orthopedic surgery for 4 patients with female pseudohermaphroditism caused by congenital adrenal hyperplasia. 目的报告4例先天性肾上腺皮质增生所致女性假两性畸形患者的激素替代治疗加手术整形的效果。
Three cases of female pseudohermaphroditism are presented. All of them are simple virilism with 21-hydroxylase deficiency caused by con-genital adrenal hyperplasia. 报道3例女性假两性畸形患者,均为单纯男性化型,系21-羟化酶缺陷所致,先天性肾上腺皮质增生引起。
Pseudohermaphroditism caused by congenital 21-hydroxylase deficiency 先天性21-羟化酶缺乏致女性假两性畸形
Objective: To improve the level of diagnosis and treatment of female pseudohermaphroditism induced by congenital adrenal hyperplasia ( CAH). 目的:提高对先天性肾上腺皮质增生所致女性假两性畸形的诊断和处理水平。
Diagnosis and treatment of female pseudohermaphroditism caused by congenital adrenal hyperplasia ( report of 4 cases) 先天性肾上腺皮质增生致女性假两性畸形的诊治(附四例报告)
Currently, some people argue that early diagnosis and comprehensive treatment are useful for treatment of some types of male pseudohermaphroditism. 目前认为,早期明确诊断,早期综合治疗对于部分类型的男性假两性畸形患者会有更好的治疗效果。
Detection of expression of T and MIS by double antibody sandwich enzyme-linked immunosorbent assay ( ELISA) and analysis the results, discussion for the meaning and relation between SRY, T, MIS and the diagnosis of male pseudohermaphroditism. 3. 对两组标本采用双抗体夹心酶联免疫吸附试验(ELISA)检测T及MIS值,对所得结果进行统计学分析,探讨SRY基因、T及MIS在男性假两性畸形诊断中的意义及相关性。
Cases of male pseudohermaphroditism with ectopic gland. 男性假两性畸形患者异位性腺8例。