Open AccessA Case of BeckwithWiedemann Syndrome with Polyhydramnios
Author(s) -
Yusrawati Yusrawati,
Reno Muhatiah
Publication year - 2017
Publication title -
indonesian journal of obstetrics and gynecology
Language(s) - English
Resource type - Journals
eISSN - 2338-7335
pISSN - 2338-6401
DOI - 10.32771/inajog.v5i3.549
Subject(s) - polyhydramnios , medicine , obstetrics , amniocentesis , caesarean section , oligohydramnios , prenatal diagnosis , fetal distress , gynecology , fetus , pregnancy , genetics , biology
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