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An extremely rare case of classic complete caudal duplication: Dipygus
Yasen Fayez Al Alayet1, Ram Samujh2, Toijam Soni Lyngdoh2
1Department of Pediatric Surgery, King Saud Medical City Children Hospital, Shemisi-Riyadh, Kingdom of Saudi Arabia.
Abstract:
Dipygus is a complete caudal duplication deformity in its severest form. The structures derived from the embryonic cloaca and notochords are duplicated to various extent. We report a male baby who presented to us with complete somatic and visceral duplication below the umbilical level associated with gastroschisis and imperforated anus. Staged surgical corrections were suggested and three out of the four stages were performed successfully.
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