Results 21 to 30 of about 54,715 (162)

Currarino triad with a duplicate anal canal presenting with an infected sacral mass

open access: yesJournal 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

open access: yesJournal 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
doaj   +1 more source

Bladder exstrophy with exstrophic rectal duplication in an infant: An extremely rare case

open access: yesAfrican 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
doaj   +1 more source

Anorectal malformation with long perineal fistula: one of a special type

open access: yesScientific 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
doaj   +1 more source

Labeling male anorectal malformations: objective evaluation of radiologic imaging before surgery

open access: yesFrontiers in Pediatrics, 2023
PurposeProne cross-table lateral x-ray (CTLxR) and colostogram aid surgical planning for anorectal malformations (ARMs) without perineal fistulas. We suggest objective imaging tools to classify ARMs.MethodsThree observers prospectively evaluated CTLxR ...
A. Morandi   +7 more
doaj   +1 more source

Frequency and Outcomes of Associated Anomalies in Anorectal Malformation in Children [PDF]

open access: yes, 2022
Background and Aim: Anorectal malformations (ARMs) are frequently occurring abnormalities in newborns. The occurrence of these issues is due to prenatal dysmorphogenesis affecting the cloaca and urorectum, leading to a significant medical concern.
Khan, M. Q. (Muhammad)   +5 more
core   +2 more sources

Experience with the management of anorectal malformations in Ibadan, Nigeria

open access: yesThe Pan African Medical Journal, 2021
INTRODUCTION: Anorectal malformation is a multi-systemic birth defect of the distal gastrointestinal tract, the management of which is challenging to the surgeons, the patients and the parents.
Olakayode Olaolu Ogundoyin   +2 more
doaj   +1 more source

Congenital heart defects in children with Gastro-intestinal malformations

open access: yesУкраїнський журнал Перинатологія і педіатрія, 2022
Background. Congenital malformations of the gastrointestinal (GI) tract are common birth defects detected in the neonatal period and usually present with signs of GI obstruction which at times can be life threatening.
A. Khanam, Sh. Abqari, R.A. Khan
doaj   +1 more source

Laparoscopic repair of long-gap rectal atresia

open access: yesJournal of Pediatric Surgery Case Reports, 2019
Long-gap rectal atresia, as defined by a distance greater than 3 cm, is an uncommon type of a rare anorectal malformation (ARM). . We report the successful completion of a 3-stage procedure including colostomy and mucous fistula creation, laparoscopic ...
Mollie Ahn   +3 more
doaj   +1 more source

POST OPERATIVE FUNCTIONAL OUTCOME FOR ANORECTAL MALFORMATIONS IN INFANT AND CHILDREN IN ERBIL [PDF]

open access: yesThe Medical Journal of Basrah University, 2020
Background/aims: Outcomes of anorectal malformations have greatly improved but many children still experience some form of urinary or fecal incontinence despite optimal management.
salar berdawd
doaj   +1 more source

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