A Case of BeckwithWiedemann Syndrome with Polyhydramnios

Suatu Kasus Sindrom Beckwith ­Wiedemann dengan Poli hidramnion

  • Yusrawati Yusrawati Faculty of Medicine Universitas Andalas/Dr. M Djamil Hospital Padang
  • Reno Muhatiah Faculty of Medicine Universitas Andalas/Dr. M Djamil Hospital Padang

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

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Author Biographies

Yusrawati Yusrawati, Faculty of Medicine Universitas Andalas/Dr. M Djamil Hospital Padang

Department of Obstetrics and Gynecology

Reno Muhatiah, Faculty of Medicine Universitas Andalas/Dr. M Djamil Hospital Padang

Department of Obstetrics and Gynecology

Published
2017-11-01
Section
Case Report