Results 141 to 150 of about 3,610 (202)

A Multicountry Analysis of Prevalence and Mortality among Neonates and Children with Bladder Exstrophy. [PDF]

Am J Perinatol
Kancherla V, Tandaki L, Sundar M, Lux A, Bakker MK, Bergman JE, Bermejo-Sánchez E, Canfield MA, Feldkamp ML, Groisman B, Hurtado-Villa P, Källén K, Landau D, Lelong N, Lopez-Camelo J, Mastroiacovo P, Morgan M, Mutchinick OM, Nance AE, Nembhard WN, Pierini A, Šípek A, Stallings EB, Szabova E, Wertelecki W, Zarante I, Rissmann A.   +26 more
europepmc   +1 more source

Bladder Exstrophy

Fetal and Pediatric Pathology, 2012
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, Guralp, Onur, Akbas, Murat, Aydin, Yavuz, Sen, Cihat, Uludag, Sezin   +5 more
core   +4 more sources

Duplicate exstrophy of the bladder

Journal of Pediatric Surgery, 1999
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.
F, Andiran, F C, Tanyel
openaire   +3 more sources

Bladder exstrophy variants.

Minerva urologica e nefrologica = The Italian journal of urology and nephrology, 2007
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, ZAMPIERI, Nicola, Pietrobelli, Angelo, GIACOMELLO, Luca, CAMOGLIO, Francesco Saverio   +4 more
core   +5 more sources

Epidemiological Survey of 214 Families With Bladder Exstrophy-Epispadias Complex

Journal of Urology, 2008
PURPOSE: We sought to identify causative nongenetic and genetic risk factors for the bladder exstrophy-epispadias complex. MATERIALS AND METHODS: A total of 237 families with the bladder exstrophy-epispadias complex were invited to participate in the ...
S Beaudoin, John P Gearhart
exaly   +2 more sources

Bladder Exstrophy

, 2009
Bladder exstrophy, more properly, the exstrophy-epispadias complex is a rare congenital anomaly occurring once every 10,000-50,000 live births with a 2.3:1 as male & female ratio. The diagnosis involves a spectrum of anomalies of the lower abdominal wall,
Amanda C. North, John P. Gearhart
openaire   +2 more sources

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Exstrophy of the bladder

Journal of Pediatric Surgery, 1969
Abstract A 20-year experience with the management of exstrophy of the bladder is presented. Follow-up data from 27 patients indicate that cystoplasty is a satisfactory operation since half of the older patients developed urinary continence with a normal upper urinary tract.
J H, Fisher, A B, Retik
openaire   +2 more sources

EXSTROPHY OF THE BLADDER

Radiologic Clinics of North America, 1977
Exstrophy of the bladder is the most common of a spectrum of related anomalies. The pelvic skeletal changes in all of these disorders vary in degree but are similar in type. The kidneys are urinary collecting systems are usually normal in patients with untreated exstrophy, and the "hurley" appearance of the lower ureters should be regarded as a ...
P, White, R L, Lebowitz
openaire   +2 more sources

Embryology of bladder exstrophy

Journal of Pediatric Surgery, 1988
A hypothesis in respect to the teratogenesis of bladder exstrophy and its variants is offered. The central feature of this hypothesis is the abnormal persistence of the caudal position of the insertion of the body stalk on the embryo. As a consequence of this, the normal advance and interposition of mesenchymal tissue to the midline becomes impossible.
H, Mildenberger, D, Kluth, M, Dziuba
openaire   +2 more sources