Results 61 to 70 of about 557 (159)

Currarino's triad diagnosed in an adult woman. [PDF]

open access: yes, 2012
_Purpose_ To report on a female patient diagnosed with Currarino's triad in adulthood. _Case report_ This case presents an adult patient with a medical history of a congenital anal atresia, a partial sacral agenesis, and a surgically treated ectopic ...
Berghauser Pont, L.M.E. (Lotte)   +2 more
core  

Variants of Currarino Syndrome: Embryological Association and Review of Pertinent Literature

open access: yesInternational Journal of Embryology, Volume 2014, Issue 1, 2014., 2014
Currarino syndrome is a triad of sacral defect, anorectal malformation and a presacral mass. The diagnosis is usually made late in childhood and about 50% of cases are familial with autosomal dominant inheritance. We present two neonates (one with vestibular fistula, and another with cloacal malformation) with the features consistent with Currarino ...
Rahul Gupta   +4 more
wiley   +1 more source

Obstetrical Outcomes in Women With a History of Bladder Augmentation

open access: yesHealth Science Reports, Volume 7, Issue 12, December 2024.
ABSTRACT Purpose To evaluate possible problems during pregnancy or delivery in women with pediatric bladder augmentation. Methods Eleven of 59 women, who had undergone bladder augmentation in our pediatric hospital during 1990–2019, had given birth in our hospital district afterwards and their obstetrical records were evaluated.
Porela‐Tiihonen Susanna   +2 more
wiley   +1 more source

Single-Stage Repair versus Traditional Repair of High Anorectal Malformations, Functional Results’ Correlation with Kelly’s Score and Postoperative Magnetic Resonance Imaging Findings [PDF]

open access: yes, 2015
Introduction: Posterior sagittal anorectoplasty (PSARP) is the standard treatment for anorectal malformations. In the present study, the clinical evaluation of anal continence was carried out using Kelly’s scoring system and the results of primary PSARP ...
Chowdhary, S   +8 more
core   +2 more sources

Single stage Anterior Sagittal Anorectoplasty (ASARP) for Anorectal Malformations with Vestibular Fistula and Perineal Ectopic Anus in Females: A New Approach

open access: yesJournal of Nepal Paediatric Society, 1970
Introduction: Despite a better understanding of the embryology, anatomy of anorectal malformations and of the physiology of continence, the management of children born with imperforate anus continues to be a surgical challenge and is still fraught with numerous complications and often leads to less than perfect qualitative results.
Pradeep B Singh   +3 more
openaire   +2 more sources

Prognostic factors for constipation following primary surgery of anorectal malformations in Yogyakarta, Indonesia [PDF]

open access: yes, 2015
Anorectal Malformation (ARM) is a congenital malformation of the anorectal area, occur approximately once in every 5000 live births. There are several morbidities could occur after surgery in ARM. Constipation is the most common morbidity post-surgery in
Marpaung, Willy Hardy, Rochadi, .
core   +3 more sources

Global Development of Research on Anorectal Malformations over the Last Five Decades: A Bibliometric Analysis [PDF]

open access: yes, 2023
Purpose: Anorectal malformations (ARM) are one of the most challenging congenital malformations in pediatric surgery. We aimed to assess the research activity on ARM over the last five decades.
Duess, Johannes W.   +5 more
core   +1 more source

Two-stage repair of low anorectal malformations in girls: is it truly a setback? [PDF]

open access: yes, 2015
Background/purpose Anorectal malformations (ARMs) affect 1 in 4000–5000 births. Low ARMs are nowadays treated in the first stage rather than at second or third stages.
Aly, K, Elsaied, A, Magdy, A, Thabet, W
core   +2 more sources

Correlation of anorectal manometry measures to severity of fecal incontinence in patients with anorectal malformations – a cross-sectional study [PDF]

open access: yes, 2020
Anorectal malformations (ARM) are a spectrum of anomalies of the rectum and anal canal affecting 1 in 2500 to 5000 live births. Functional problems are common and related to the type of ARM and associated malformations.
Baatrup, G.   +4 more
core   +1 more source

Repair of “bladder neck” cloaca using a trans-vesicle approach: A case report

open access: yesJournal of Pediatric Surgery Case Reports
Introduction: Cloaca with a common channel greater than 3 cm typically requires urogenital separation rather than total urogenital mobilization. The purpose of this report was to describe our experience managing a female infant with an usual form of ...
Nathalie Carey   +4 more
doaj   +1 more source

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