BACKGROUND Complete colonic duplication is a very rare congenital anomaly that may have different presentations according to its location and size. Complete colonic duplication can occur in 15% of gastrointestinal duplication. We report two cases of complete colonic duplications, and their characteristics. CASE PRESENTATION We present two patients with complete colonic duplication with differ...

SUMMARY An infant is reported with imperforate anus and complete duplication of colon, rectal pouch, doubling of the genitalia with completely formed penes, double bladder and urethra. This 2 days old male was operated on several times, but finally expired on 33 days old with respiratory disorder and sepsis.

Background: Complete colonic duplication is a very rare congenital anomaly that may have different presentations according to its location and size. Complete colonic duplication can occur in 15% of gastrointestinal duplication. We report two cases of complete colonic duplications, and their characteristics. Case Presentation: We present two patients with complete colonic duplication with differ...

background: complete colonic duplication is a very rare congenital anomaly that may have different presentations according to its location and size. complete colonic duplication can occur in 15% of gastrointestinal duplication. we report two cases of complete colonic duplications, and their characteristics. case presentation: we present two patients with complete colonic duplication with differ...

introduction: penile agenesis (pa) and diphallus (dp) are extremely rare genital anomaly in children. numerous associated anomalies have been described with these malformations. these patients need several investigations and finally surgical intervention.   material & methods: in a retrospective study, 14 patients who were treated for phallus malformation in mofid children’s hospital from janua...