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- W2183451372 abstract "Background :Penile duplication (diphallus) is an extremely rare disorder. It is almost always associated with other malformations like d ouble bladder, exstrophy of the cloacae, imperforate anus, duplication of the rectosigmoid and vertebral deformities. Meanwhile anal canal duplication, the most distal and least common duplication of the digestive tube and is a very rare congenital malform ation. Case Presentation:A 21 days old Egyptian neonate is reported with complete penile duplication and two scrotums with each one carrying two palpable testes. Both peniseshave normal shaft with normally located meatus. Clear urine voids from both meat i spontaneously. The child had also a fold of redundant skin about 4◊5 cm at the anal region in which two separate anal openings are present. In rectalexamination we found two normal anuses passing stool spontaneously. Ascending (voiding) cystourethrograp hy revealed two penises with two separate meatuses and one bladder from which the two urethrasgo outseparately. Intravenous pyelogram (IVP) revealed two normal kidneys and ureters. Barium study revealed duplication of rectum and colon, otherwise normal G IT. Conclusion:In our review of the literature, we did not come across any other case of this variety of the penile duplication and congenital presence of two an uses. Unfortunatelythe patientexpired before any surgical correction." @default.
- W2183451372 created "2016-06-24" @default.
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- W2183451372 date "2012-01-01" @default.
- W2183451372 modified "2023-09-27" @default.
- W2183451372 title "Penile Duplicationand Two Anal Opening s; Report of aVery Rare Case" @default.
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