A Case of BeckwithWiedemann Syndrome with Polyhydramnios
AbstractObjective: 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
How to Cite
YUSRAWATI, Yusrawati; MUHATIAH, Reno. A Case of BeckwithWiedemann Syndrome with Polyhydramnios. Indonesian Journal of Obstetrics and Gynecology (INAJOG), [S.l.], p. 185-188, nov. 2017. ISSN 2338-7335. Available at: <http://inajog.com/ojs/index.php/journal/article/view/549>. Date accessed: 16 dec. 2017.