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

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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.

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            Author and article information

            Journal
            10.54878/IJATMS
            International Journal of Applied Technology in Medical Sciences
            IJATMS
            Emirates Scholar
            24 November 2022
            : 1
            : 1
            : 18-23
            Affiliations
            [1 ]Armed Forces Hospital, Saudi Arabia
            Author notes
            Correspondence: Ohayla Elhag ( ohayla998@ 123456gmail.com )
            Article
            10.54878/IJATMS.207
            532b53b5-7249-4f6c-98e7-2b3b15b41dc4
            ©2022Emirates Scholar

            This is an open access article published by Emirates Scholar and distributed under the Creative Commons Attribution License 4.0 (CC BY).

            History

            Nursing,Surgery,Internal medicine,Pharmacology & Pharmaceutical medicine,Health & Social care,Public health
            Mayer-Rokitansky-Kuster-Hauser Syndrome, Renal Insufficiency, Congenital Anomaly, Bilateral Renal Agenesis, BPD & HC, Potter Syndrome

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