Case Report of Bilateral renal agenesis (Potter s syndrome) at 26 weeks gestational age.

S. Hassan, Ohayla Hassan, Hassan Himt
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Abstract

Case report: 19 years old PG married for 1 year, her husband is her cousin. No family history of congenital anomalies, No significant past medical history nor drug history. She as referred for anomaly scan, the pregnancy was uneventful till referral she was on good antenatal care received folic acid supplement. Ultrasound findings: Single, viable, breech presentation. Posterior high placenta Anhydramnios GA by ultrasound 26+3days (HC:28+6, FL:24+3, AC: 24+4) Congenital anomalies: Hydrocephalus (severe ventriculomegaly measuring 22cm, normal is <10cm Dilated third ventricle (6mm) thalami are not seen well. Both kidneys show features of multicystic changes No cortico-medullary differentiation. Bladder filling is not seen Conclusion A picture suggestive of bilateral non-functioning kidneys. Hydrocephalus. No major anomaly seen however other anomalies can’t be excluded due to poor visualization. Impressionvery poor outcome.
孕26周双侧肾发育不全(波特综合征)1例。
病例报告:19岁PG结婚1年,丈夫为表兄弟。无先天性异常家族史,无重大既往病史和用药史。她被转诊为异常扫描,妊娠顺利,直到转诊,她得到良好的产前护理,接受叶酸补充。超声表现:单一,活的,臀位表现。先天性异常:脑积水(严重脑室增大22cm,正常<10cm),第三脑室扩张(6mm),丘脑未见明显。双肾呈多囊性改变,无皮质-髓质分化。结论提示双侧肾功能不全,脑积水,未见明显异常,但因视觉不良不能排除其他异常。印象非常差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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