假两性畸形

jiǎ liǎnɡ xìnɡ jī xínɡ
  • pseudohermaphroditism
假两性畸形假两性畸形
  1. 女性假两性畸形:由白细胞的初步分析,认为可能是XO(45)/XY(46)嵌合体。

    Female pseudohermaphroditism ( 1 case ) . A preliminary analysis of the patient revealed the possibility of being an XO ( 45 ) / XY ( 46 ) mosaic .

  2. 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。

    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 .

  3. 药物性女性假两性畸形矫治13例分析

    Correction for female pseudohermaphroditism in 13 patients caused by extraneous androgen

  4. 本文报告5例女性假两性畸形,系由于肾上腺皮质21羟化酶缺乏致先天性肾上腺皮质增生引起。

    Five cases of female pseudohermaphroditism caused by 21-hydroxylase deficiency were reported .

  5. 同胞中两人患不完全性男性假两性畸形Ⅱ型的病例报告

    A clinical report on the sibling with imcomplete male pseudohermaphroditism

  6. 肾上腺皮质21羟化酶缺乏症(附5例女性假两性畸形报告)

    Adrenal 21-Hydroxylase Deficiency ( Report of Five Female Pseudohermaphroditism )

  7. 还发现2例男性假两性畸形其性染色体正常,但常染色体分别为臂间倒位及13和14号染色体间的易位时,也可以导致性别异常。

    The abnormalities in 9,13 and 14 chromosomes resulted in intersex also .

  8. 目的评价女性假两性畸形的影像学特点。

    Objective To evaluate the imaging features of female pseudohermaphroditism .

  9. 方法回顾性分析9例女性假两性畸形的影像资料。

    Methods The imaging findings in9 cases of female pseudohermaphroditism were analyzed retrospectively .

  10. 21羟化酶缺乏致女性假两性畸形的治疗效果

    Combined treatment of female pseudohermaphroditism caused by 21-hydroxylase deficiency

  11. 男性假两性畸形患者异位性腺8例。

    Cases of male pseudohermaphroditism with ectopic gland .

  12. 先天性21-羟化酶缺乏致女性假两性畸形

    Pseudohermaphroditism caused by congenital 21 - hydroxylase deficiency

  13. 女性假两性畸形三例报告

    Female Pseudohermaphroditism & A Report of 3 Cases

  14. 带蒂皮瓣一期成形矫治男性假两性畸形

    One-stage repair of male pseudohermaphroditism with butterfly-shaped flap from labia majora and vulva rima

  15. 26例女性假两性畸形分析

    Analysis of 26 cases of female pseudohermaphroditism

  16. 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 .

  17. 假两性畸形的诊断和治疗

    Diagnosis and Treatment of Pseudohermaphroditism

  18. 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)

    Diagnosis and treatment of female pseudohermaphroditism caused by congenital adrenal hyperplasia ( report of 4 cases )

  19. 目的探讨女性假两性畸形的诊断和治疗的时机及方法。

    Objective To investigate the optimal time and best way for diagnosing and treating female adrenogenital syndrome .

  20. 5α-还原酶2型缺乏,会导致男性假两性畸形和其他相关的临床表现。

    5 α - reductase type 2 deficiency in male lead to male pseudohermaphroditism and other related phenotypes .

  21. 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。

    Currently , some people argue that early diagnosis and comprehensive treatment are useful for treatment of some types of male pseudohermaphroditism .

  22. 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。

    Objective : To improve the level of diagnosis and treatment of female pseudohermaphroditism induced by congenital adrenal hyperplasia ( CAH ) .

  23. 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。

    Objective To report the effect of hormone replacement plus orthopedic surgery for 4 patients with female pseudohermaphroditism caused by congenital adrenal hyperplasia .

  24. 结果47名患者临床确诊为男性假两性畸形,其中31名患者通过实验室、影像学等检查进一步明确病因学诊断。

    Results Etiologic diagnosis had been made for 31 of the 47 patients with the help of laboratory examination , ultrasonic and radiological examination .

  25. 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。

    Three cases of female pseudohermaphroditism are presented . All of them are simple virilism with 21-hydroxylase deficiency caused by con - genital adrenal hyperplasia .

  26. 结论根据畸形特征设计的Prader5型女性假两性畸形矫治手术新颖、科学、操作简单、对患者损伤小,效果好,值得推广;

    Conclusion The orthomorphia of Prader type 5 designed according to deformity properties is new , scientific and simple with less damage to patients and better effects . It is worth popularizing .

  27. 先天性肾上腺皮质增生为女性假两性畸形的最常见类型,7例,包括21-羟化酶缺陷5例和17α羟化酶缺陷2例,其中1例17α羟化酶缺陷睾丸有恶变;

    Congenital adrenal hyperplasia was the most familiar of female pseudohermaphroditism , 5 were 21-Hydroxylase Deficiency and 2 were 17 α - Hydroxylase Deficiency , and the testicle of one 17 α - Hydroxylase Deficiency occurred canceration .