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- W2896742445 abstract "Objective: To report a rare case of Beckwith-Wiedemann Syndrome with polyhydramnios.
 Methods: Reporting a case of Beckwith-Wiedemann syndrome with polyhydramnios.
 Results: Case of Mrs. Y, 27 years old woman, G2P1A0L1 preterm pregnancy (30-31 weeks) with polyhidramnios. From ultrasound found renomegaly, bilateral hyperechogenic polycystic kidney, and the karyotype result was 46,XX. Caesarean section was performed due to fetal distress. A female baby was born by caesarean section with birth weight of 1300 grams, 37 centimeters of body length, and APGAR score of 6/8. The congenital anomalies found were hepatomegaly, renomegaly, bilateral hyperechogenic renal polycystic, low set ears. The baby was died in NICU on day care 5th, with suspected of sepsis.
 Conclusion: Prenatal diagnosis of Beckwith-Wiedemann syndrome on fetus with polyhydramnios.
 [Indones J Obstet Gynecol 2017; 5-3: 185-188]
 Keywords: amniocentesis, beckwith-wiedemann syndrome, polyhydramnios, prenatal diagnostic, USG" @default.
- W2896742445 created "2018-10-26" @default.
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- W2896742445 date "2017-11-01" @default.
- W2896742445 modified "2023-09-25" @default.
- W2896742445 title "A Case of BeckwithWiedemann Syndrome with Polyhydramnios" @default.
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- W2896742445 doi "https://doi.org/10.32771/inajog.v5i3.549" @default.
- W2896742445 hasPublicationYear "2017" @default.
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