A research report submitted to the Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, in partial fulfilment of the requirements for the degree of Master of Medicine in Paediatrics Johannesburg, 2017Background: PBS is a rare congenital disorder with a triad of signs: absent abdominal wall musculature, urinary tract malformations, cryptorchidism. Objectives: Describe the patient profile, management, and outcome of patients attending the Paediatric Nephrology clinic at Chris Hani Baragwanath Academic Hospital. Methods: Retrospective descriptive record review. Results: 44 patient files were analysed. Median duration of follow up: 24 months (1.7–130). Median age at presentation was 5.5 days (1–730). Associated conditi...
Prune belly syndrome (PBS) also known as Eagle Barret syndrome is a rare congenital disorder that is...
Prune belly syndrome (PBS) is a rare congenital disorder affecting 2.5 to 3.8/100,000 live births wo...
Prune-Belly syndrome is a rare congenital disorder, and in underdeveloped and developing countries, ...
Background: Prune belly syndrome (PBS) is a rare congenital disorder with a triad of signs: absent a...
Background: Prune belly syndrome (PBS) is a rare congenital malformation of unclear etiology. The di...
Background: Prune-Belly syndrome, Eagle-Barret syndrome and triad syndrome, all refer to congenital ...
Prune Belly Syndrome (PBS) is a rare congenital syndrome characterized by three main features: abdom...
Prune Belly Syndrome is a rare congenital disorder with unknown aetiology, consisting of a triad of ...
As outcome data for prune belly syndrome (PBS) complicated by end-stage renal disease are scarce, we...
AbstractThe triad of deficient abdominal wall musculature, undescended testes and urinary tract anom...
Background: Prune belly Syndrome is a rare congenital disorder made up of a myriad of anomalies with...
Objective: Review outcomes of Prune Belly Syndrome (PBS) with the hypothesis that contemporary manag...
The Prune-Belly syndrome (PBS) is a rare pathology predominating in male infants, classically manife...
We describe a 2-year-old boy seen in Kenya who presented with fever, dysuria, foul smelling urine, a...
As outcome data for prune belly syndrome (PBS) complicated by end-stage renal disease are scarce, we...
Prune belly syndrome (PBS) also known as Eagle Barret syndrome is a rare congenital disorder that is...
Prune belly syndrome (PBS) is a rare congenital disorder affecting 2.5 to 3.8/100,000 live births wo...
Prune-Belly syndrome is a rare congenital disorder, and in underdeveloped and developing countries, ...
Background: Prune belly syndrome (PBS) is a rare congenital disorder with a triad of signs: absent a...
Background: Prune belly syndrome (PBS) is a rare congenital malformation of unclear etiology. The di...
Background: Prune-Belly syndrome, Eagle-Barret syndrome and triad syndrome, all refer to congenital ...
Prune Belly Syndrome (PBS) is a rare congenital syndrome characterized by three main features: abdom...
Prune Belly Syndrome is a rare congenital disorder with unknown aetiology, consisting of a triad of ...
As outcome data for prune belly syndrome (PBS) complicated by end-stage renal disease are scarce, we...
AbstractThe triad of deficient abdominal wall musculature, undescended testes and urinary tract anom...
Background: Prune belly Syndrome is a rare congenital disorder made up of a myriad of anomalies with...
Objective: Review outcomes of Prune Belly Syndrome (PBS) with the hypothesis that contemporary manag...
The Prune-Belly syndrome (PBS) is a rare pathology predominating in male infants, classically manife...
We describe a 2-year-old boy seen in Kenya who presented with fever, dysuria, foul smelling urine, a...
As outcome data for prune belly syndrome (PBS) complicated by end-stage renal disease are scarce, we...
Prune belly syndrome (PBS) also known as Eagle Barret syndrome is a rare congenital disorder that is...
Prune belly syndrome (PBS) is a rare congenital disorder affecting 2.5 to 3.8/100,000 live births wo...
Prune-Belly syndrome is a rare congenital disorder, and in underdeveloped and developing countries, ...