Journal
Case Report of Bilateral renal agenesis (Potter s syndrome) at 26 weeks gestational age.
المستخلص
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
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
الكلمات المفتاحية
Bilateral Renal Agenesis
BPD & HC
Congenital Anomaly
Mayer-Rokitansky-Kuster-Hauser Syndrome
Renal Insufficiency
Potter Syndrome
