Duplicate bladder exstrophy with hypospadias: A rare exstrophy variant with unusual association
نویسندگان
چکیده
منابع مشابه
True Duplicate Bladder Exstrophy
A three months male child was admitted in our department as a rare variant of bladder exstrophy (true duplicate bladder exstrophy). There are only 8 cases of this variant reported in the literature so far, we report an additional case to add the scarce literature.
متن کاملExstrophy Bladder with Low Anorectal Malformation- A Rare Association
A 4-day-old male newborn, weighing 2.5 Kg, delivered vaginally at 38 weeks presented with malformed external genitalia and a reddish swelling over the lower part of the abdomen and the absent anal opening with a small perineal opening. Pregnancy was uneventful. Maternal serologies for HbsAg, HCV, HIV, Toxoplasma, and Rubella were planned but due to financial reason not done. Physical examinatio...
متن کاملCounseling Pregnant Women with Bladder Exstrophy
Background: Bladder exstrophy is a very rare congenital anomaly characterized by a defect in the closure of the lower abdominal wall and eversion of the bladder mucosa, ureteral orifices, bladder neck, and urethra Case : A 37-year-old woman arrived at the emergency room with a missed abortion. She was para 5-0-3-1 and had a breech section 7 years earlier. Conclusion: We describe patients with b...
متن کاملBladder Exstrophy and Epispadias
Introduction Exstrophy and epispadias are part of a spectrum of anomalies characterised by exposure of part or all of the mucosa of the lower urinary tract (bladder and urethra) to the external environment through a defect in the anterior abdominal wall. At one end of this spectrum is cloacal exstrophy, which is the most complex of these anomalies. It is characterised by exposure of the bladder...
متن کاملBladder exstrophy-epispadias complex.
The bladder exstrophy-epispadias complex (BEEC) represents an anterior midline defect with variable expression comprising a spectrum of anomalies involving the abdominal wall, pelvis, urinary tract, genitalia, and occasionally the spine and anus. The vast majority of BEEC cases are classified as non-syndromic and the etiology of this malformation is still unknown. This review presents the curre...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Journal of Indian Association of Pediatric Surgeons
سال: 2017
ISSN: 0971-9261
DOI: 10.4103/0971-9261.207625