Results 11 to 20 of about 4,923 (199)
Iranian Journal of Pediatric Surgery, 2020 Introduction: Anorectal malformation [ARM] can be treated either by staged procedures or by a single stage procedure. In the present study we have performed single stage surgery of ARM in male neonates.
Vinit Kumar Thakur +5 more
doaj +3 more sources
Rare anorectal malformation with a non-terminal colovesical fistula
Journal of Pediatric Surgery Case Reports, 2015 We describe a unique case of anorectal malformation (ARM) with a non-terminal colovesical fistula. While some aspects are similar to the congenital pouch colon (CPC), the differences make it a distinct form.
Sabine Vasseur Maurer +3 more
doaj +2 more sources
Association of anorectal malformation with anal and rectal duplication
Acta Pediátrica de México, 2014 The objective of this paper is to report our experience in the diagnosis and therapy of rectal and anal duplications, all associated to anorectal malformation.
Karla A. Santos-Jasso +1 more
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Anorectal Malformation: An Atypical Association of Pierre Robin Sequence [PDF]
Pediatric Sciences Journal, 2022 Isolated Pierre Robin sequence (PRS) is characterized by underdeveloped jaw, backward displacement of the tongue and upper airway obstruction with or without cleft palate or be part of a known syndrome as VACTREL or CHARGE, or be associated with other ...
Manal M. Farouk +2 more
doaj +1 more source
Orphanet Journal of Rare Diseases, 2006 Anorectal malformations comprise a wide spectrum of diseases, which can affect boys and girls, and involve the distal anus and rectum as well as the urinary and genital tracts. They occur in approximately 1 in 5000 live births. Defects range from the very minor and easily treated with an excellent functional prognosis, to those that are complex ...
Peña Alberto, Levitt Marc A
openaire +4 more sources
Clinics in Colon and Rectal Surgery, 2018 Abstract This chapter provides a review of the diagnosis and management of anorectal malformations. It describes the initial workup and care in the newborn period, as well as the indications and techniques for initial surgical intervention, if required, and definitive reconstructive surgery.
Richard J, Wood, Marc A, Levitt
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Currarino triad with a duplicate anal canal presenting with an infected sacral mass
Journal of Pediatric Surgery Case Reports, 2022 Currarino syndrome is a rare congenital malformation characterised by the triad of: an anorectal malformation, sacral bony defect and presacral mass. One rare but possible anorectal malformation is an anal canal duplication, a congenital anomaly which is
Sun Woo Lee +4 more
doaj +1 more source
Delayed diagnosis of congenital anorectal malformation
Journal of Pediatric Surgery Case Reports, 2020 Background: Congenital anorectal malformation is uncommon and often missed-diagnosed. The diagnosis can be late due to late presentation of the complaint.
Daniel Ardian Soeselo +2 more
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Bladder exstrophy with exstrophic rectal duplication in an infant: An extremely rare case
African Journal of Paediatric Surgery, 2021 Exstrophic rectal duplication and its association with bladder exstrophy and anorectal malformation is an extremely rare clinical entity. This is a report of the second case of an exstrophic rectal duplication associated with bladder exstrophy in English
Levent Duman +2 more
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Anorectal malformation with long perineal fistula: one of a special type
Scientific Reports, 2021 The anorectal malformation with long perineal fistula is a rare anomaly in the spectrum of anorectal malformations. Aim of the study is to describe the series of patients with anorectal malformation with long perineal fistula and compare the outcome with
Sen Li, Jun Wang
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