scholarly journals Severe Bladder Outlet Obstruction in a 7-Week-Old Infant Presenting with Features of Prune Belly Syndrome: A Case Report

2020 ◽  
Vol 7 (1) ◽  
Author(s):  
Muhammad Sule Baba
Keyword(s):  
Case Report ◽  
Bladder Outlet Obstruction ◽  
Outlet Obstruction ◽  
Prune Belly Syndrome ◽  
Prune Belly

Early bladder outlet obstruction in fetal lambs induces renal dysplasia and the prune-belly syndrome

1990 ◽  
Vol 25 (3) ◽  
pp. 342-345 ◽  
Author(s):  
Ricardo Gonzalez ◽  
Yuri Reinberg ◽  
Barbara Burke ◽  
Thomas Wells ◽  
Robert L. Vernier
Keyword(s):  
Bladder Outlet Obstruction ◽  
Outlet Obstruction ◽  
Renal Dysplasia ◽  
Prune Belly Syndrome ◽  
Prune Belly

scholarly journals Living-related kidney transplantation with catheterizable urinary conduit in prune belly syndrome: A case report

2018 ◽  
Vol 51 ◽  
pp. 150-153 ◽  
Author(s):  
Taro Banno ◽  
Yoichi Kakuta ◽  
Kohei Unagami ◽  
Akiko Sakoda ◽  
Masayoshi Okumi ◽  
...  
Keyword(s):  
Kidney Transplantation ◽  
Case Report ◽  
Prune Belly Syndrome ◽  
Prune Belly ◽  
Living Related

scholarly journals PRUNE-BELLY SYNDROME IN 2 CASES SEEN IN A TERTIARY MEDICAL INSTITUTION SOUTHEAST NIGERIA – A CASE REPORT

2019 ◽  
Vol 6 (6) ◽  
pp. 331-334
Author(s):  
Muoneke Vivian Uzoamaka ◽  
Nwokoye Ikenna ◽  
Ezeanosike Obumneme ◽  
Onyire Nnamdi Benson ◽  
Nwokeji-Onwe Linda ◽  
...  
Keyword(s):  
Case Report ◽  
Medical Institution ◽  
Prune Belly Syndrome ◽  
Prune Belly

scholarly journals Anesthetic Management of Prune-Belly Syndrome: Case Report

2015 ◽  
Vol 23 (3) ◽  
pp. 215-219
Author(s):  
Tuğçe BARÇA ŞEKER ◽  
Ayşe Çiğdem TÜTÜNCÜ
Keyword(s):  
Case Report ◽  
Anesthetic Management ◽  
Prune Belly Syndrome ◽  
Prune Belly

scholarly journals Prune belly syndrome in an Egyptian infant with Down syndrome: A case report

2008 ◽  
Vol 2 (1) ◽  
Author(s):  
Kotb A Metwalley ◽  
Hekma S Farghalley ◽  
Alaa A Abd-Elsayed
Keyword(s):  
Down Syndrome ◽  
Case Report ◽  
Prune Belly Syndrome ◽  
Prune Belly

Prenatal Diagnosis of Prune Belly Syndrome: A Case Report

2021 ◽  
Author(s):  
Shivya Parashar ◽  
Rajesh Malik ◽  
Radha S. Gupta ◽  
Kamaljeet S. Randhawa
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Prune Belly Syndrome ◽  
Prune Belly

scholarly journals Complex Cardiac Defect in a Fetus with Trisomy 18: A Case Report

2017 ◽  
Vol 02 (01) ◽  
pp. 068-071
Author(s):  
Shagun Aggarwal
Keyword(s):  
Case Report ◽  
Bladder Outlet Obstruction ◽  
Outlet Obstruction ◽  
Esophageal Stenosis ◽  
Trisomy 18 ◽  
Cardiac Defect ◽  
Edwards Syndrome ◽  
The Family ◽  
Syndromic Diagnosis ◽  
Antenatal Detection

AbstractThis is a case report of a foetus which was brought for postmortem evaluation following antenatal detection of a complex cardiac defect. Presence of dysmorphism and other malformations like gut malrotation, bladder outlet obstruction, and esophageal stenosis led to suspicion of a syndromic diagnosis. Fetal karyotyping confirmed a diagnosis of Trisomy 18 (Edwards syndrome). This facilitated appropriate genetic counseling of the family and guidance for prenatal diagnosis in subsequent pregnancies.

The Mechanism of Prune Belly Syndrome Development: A Sonographic Sequential Assessment

2020 ◽  
Vol 36 (6) ◽  
pp. 594-603
Author(s):  
Raham Bacha ◽  
Syed Amir Gilani ◽  
Iqra Manzoor ◽  
Iftikhar Ahmad ◽  
Syed Faisal Hanan Shah
Keyword(s):  
Abdominal Wall ◽  
Anterior Abdominal Wall ◽  
Outlet Obstruction ◽  
Normal Karyotype ◽  
Abdominal Distention ◽  
Ductus Venosus ◽  
Prune Belly Syndrome ◽  
Prune Belly ◽  
Antenatal Sonography ◽  
Urinary Tract Malformations

Prune belly syndrome is a rare disorder characterized by the absence of anterior abdominal wall muscles, bilateral cryptorchidism, and urinary tract malformations. The aim of this case study was to illustrate the developmental sequelae of prune belly syndrome, acquired through a series of antenatal sonography. A 20-year-old woman visited a diagnostic medical sonography center for an obstetrical sonogram. Her fetus was diagnosed with megacystis at 15 weeks’ gestation. The mother returned for repeated appointment and to observe fetal changes during the development of prune belly syndrome. First, the megacystis, hydroureter, and hydronephrosis were noted followed by hazy ascitic and amniotic fluid. The hemodynamics were altered in the umbilical artery, middle cerebral artery, and ductus venosus. Subsequently, the pressure was neutralized, but it was observed after birth that the newborn had cryptorchidism, a distended abdomen with wrinkled wall, and absent right kidney. In conclusion, prune belly syndrome could be caused by megacystis due to bladder outlet obstruction in otherwise normal karyotype fetuses. Megacystis leads to hydroureter, hydronephrosis, and abdominal distention. The persistent abdominal distention gives rise to the underdevelopment of anterior abdominal wall muscles and cryptorchidism.

Prenatal Diagnosis of “Prune Belly” Syndrome: Case Report

1981 ◽  
Vol 146 (10) ◽  
pp. 717-718
Author(s):  
Arthur C. Wittich ◽  
Charles R. Cochrane ◽  
Jenny E. Brockdorff
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Prune Belly Syndrome ◽  
Prune Belly
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