Successful vaginal delivery in a patient with reconstructed bladder exstrophy and vaginoplasty after cesarean section, a case report from Syria. [PDF]
Balouli M +5 more
europepmc +1 more source
Radiographic calibration for pubic diastasis assessment in bladder exstrophy-epispadias complex: a phantom study. [PDF]
Back SJ +8 more
europepmc +1 more source
Modified penile reconstruction in classic bladder exstrophy: Can complete corporal covering of the urethral closure be achieved using incomplete disassembly technique? [PDF]
Nikolaev VV, Demin NV.
europepmc +1 more source
De novo variants identified by trio whole exome sequencing of bladder exstrophy epispadias complex. [PDF]
Jelin AC +10 more
europepmc +1 more source
Optimizing prenatal diagnosis and referral of classic bladder exstrophy: Lessons from a single-institution experience. [PDF]
Hirsch AM +6 more
europepmc +1 more source
Innervation pattern of the unclosed detrusor muscle in classic bladder exstrophy: a study of patients with urothelial overexpression of nerve growth factor. [PDF]
Promm M +7 more
europepmc +1 more source
Bladder exstrophy is a very rare congenital malformation in which the anterior wall of the bladder is absent, and the posterior wall is exposed externally. The differential diagnosis includes omphalocele, gastroschisis, and cloacal exstrophy. Ultrasound and Doppler examinations are the main diagnostic tools.
Uludag, Seyfettin +5 more
core +4 more sources
Duplicate exstrophy of the bladder
Duplicate exstrophy of the bladder is a rare, distinct congenital anomaly without additional major anomalies of the urinary tract. A 15-year-old boy with duplicate exstrophy is reported on, and the possible role of bladder sequestration in the development of classical musculoskeletal deformities in this anomaly is discussed.
Tanyel, FERİDUN CAHİT, Andiran, F
openaire +4 more sources
In the literature it is possible to find many case reports of bladder exstrophy variants, although a thorough classification with all possible associated malformations is not yet available. On the basis of a rare case observed at their Department, the authors studied the embryology of these conditions and their associated malformations.
CORROPPOLO, Michele +4 more
core +6 more sources

