scholarly journals VP52.06: Prenatal diagnosis of the rare case of diphallia in association with bladder exstrophy

2021 ◽  
Vol 58 (S1) ◽  
pp. 308-308
Author(s):  
H. Vafaei ◽  
S. Roozmeh ◽  
A. Bahador ◽  
M. Zare Khafri ◽  
M. Ghiasi ◽  
...  
Author(s):  
Yusrawati Yusrawati ◽  
Reno Muhatiah

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


2018 ◽  
Vol 52 ◽  
pp. 213-213
Author(s):  
H. Muñoz ◽  
C. Cabrera ◽  
Y. Copado Mendoza ◽  
G. Munoz ◽  
N. Cornejo ◽  
...  

2012 ◽  
Vol 94 (4) ◽  
pp. 245-248 ◽  
Author(s):  
Stavros Sifakis ◽  
Katherine Anagnostopoulou ◽  
Konstantina Plastira ◽  
Nikolaos Vrachnis ◽  
Anastasia Konstantinidou ◽  
...  

2012 ◽  
Vol 52 (2) ◽  
pp. 111-114 ◽  
Author(s):  
Zeki Sahinoglu ◽  
Arif Aktug Ertekin ◽  
Aysenur Cerrah Celayir ◽  
Berrin Gucluer

1990 ◽  
Vol 162 (3) ◽  
pp. 675-678 ◽  
Author(s):  
Richard Jaffe ◽  
Alex Schoenfeld ◽  
Jardena Ovadia

1999 ◽  
pp. 259-261 ◽  
Author(s):  
ALFREDO CACCIARI ◽  
GIAN LUIGI PILU ◽  
MAURIZIO MORDENTI ◽  
PIER LUCA CECCARELLI ◽  
GIOVANNI RUGGERI

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