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Journal of Pediatric Surgery
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    • Udassin, RaphaelRemove Udassin, Raphael filter
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    • Arbell, Dan1
    • Gur, Ilan1
    • Kaliner, Ehud1
    • Mazeh, Haggi1
    • Naveh, Yaron1
    • Orkin, Boris1

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    • Journal of Pediatric Surgery2

    Keyword

    • Absent dorsal mesentery1
    • Choledochal cyst1
    • Duodenojejunal atresia1
    • Recurrent1
    • Volvulus1

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    • Rapid Communication

      Three recurrent episodes of malrotation in an infant

      Journal of Pediatric Surgery
      Vol. 42Issue 4e1–e3Published in issue: April, 2007
      • Haggi Mazeh
      • Ehud Kaliner
      • Raphael Udassin
      Cited in Scopus: 10
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        Malrotation with midgut volvulus in a newborn is not a rare condition and Ladd's procedure is the recommended surgical treatment. Recurrent volvulus after Ladd's procedure is very rare. We present a case of an infant operated on after birth for malrotation and midgut volvulus with 2 recurrent similar episodes in the following 20 months. We recommend abrasion of the parietal and visceral peritoneal surfaces when recurrence of malrotation occurs.
        Three recurrent episodes of malrotation in an infant
      • Rapid Communication

        Duodenojejunal atresia with absent dorsal mesentery, choledochal cyst, and malrotation in a premature newborn—a case report

        Journal of Pediatric Surgery
        Vol. 41Issue 6e11–e13Published in issue: June, 2006
        • Dan Arbell
        • Boris Orkin
        • Yaron Naveh
        • Ilan Gur
        • Raphael Udassin
        Cited in Scopus: 17
        Online Only
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          We present the case of a premature baby who was born with the following conditions: an extensive atresia from the first part of the duodenum to the mid small bowel; malrotation of the distal part, in volvulus and in an “apple peel” configuration; no connection of the bile ducts to the bowel; and presence of a type II choledochal cyst. To our knowledge, this is the first case in which a combination of these anomalies is reported. A brief review of the relevant literature is also presented.
          Duodenojejunal atresia with absent dorsal mesentery, choledochal cyst, and malrotation in a premature newborn—a case report
        Page 1 of 1

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