45 X/46 XY核型混合性性腺发育不良伴主动脉缩窄1例。

A Büyükgebiz, H Oren, E Unsal, A Akçoral, E Ozen, M Sakizli
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引用次数: 0

摘要

我们报告一例混合性性腺发育不良与45 X/46 XY核型和主动脉缩窄。一个8个月大的病人被接纳到我们的内分泌科评估模糊的生殖器。体格检查,颈部宽,后发际线低,阴囊分裂,阴茎小,右侧阴唇襞睾丸,单口,主动脉缩窄的典型表现。患者染色体核型为45x / 46xy。剖腹检查显示婴儿子宫、输卵管和左侧的条纹性腺。患者的随访包括性别分配、生殖器重建和心血管治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of mixed gonadal dysgenesis with 45 X/46 XY karyotype and aortic coarctation.

We report a case of mixed gonadal dysgenesis with 45 X/46 XY karyotype and aortic coarctation. An eight month-old patient was admitted to our endocrinology department for evaluation of ambiguous genitalia. On physical examination, a wide neck with a low posterior hairline, bifid scrotum, small phallus, testis in the right labioscrotal fold, single orifice and typical findings of aortic coarctation were present. The chromosome karyotype of the patient was 45 X/46 XY. On the laparotomy there was an infantile uterus, fallopian tubes, and a streak gonad on the left. The follow-up of the patient included sex assignment, genital reconstruction and cardiovascular treatment.

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