Results 21 to 30 of about 1,588 (212)
Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence:two case reports and a review of the literature [PDF]
Background: The vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association and Mayer-Rokitansky-Küster-Hauser syndrome are rare conditions.
Bjørsum-Meyer, T. +3 more
core +3 more sources
We present a case of a 6-month-old male infant with an anorectal malformation (ARM) who underwent colostomy as a newborn, and now presents for definitive repair.
Anisha Apte +2 more
doaj +1 more source
Esophageal Heterotopic Pancreas in an Asymptomatic 2‐Year‐Old With VACTERL Association
A 2‐year‐old male with VACTERL association and asthma presented to the emergency room due to asthma exacerbation. Chest radiography revealed lingular pneumonia and thickening of the left paraspinal line of the gastroesophageal junction. Chest computed tomography confirmed a heterogeneous fluid‐ and gas‐filled structure at the left posterior lateral ...
Kathryn M. Kimsey +6 more
wiley +1 more source
Introduction: High and intermediate types of anorectal malformations (ARMs) may be managed by either open posterior sagittal anorectoplasty (PSARP) or by laparoscopic-assisted anorectoplasty (LAARP).
Chhabi Ranu Gupta +6 more
doaj +1 more source
Multidisciplinary strategies for managing acute watery diarrhea in children with congenital anorectal malformation and colostomy. Key clinical message Congenital anorectal malformation (ARM) is a diverse group of anomalies affecting the development of the anal and rectal regions, with an estimated incidence of one in every 5000 live births.
Mohammad Ashraful Amin +3 more
wiley +1 more source
Abstract Anorectal malformation (ARM) is a common congenital gastrointestinal malformation in neonates, which has complex pathological changes and unclear etiology. The only treatment modality currently available for ARMs is through surgical treatment to correct the deformity of the anal morphology and restore normal defecation function.
Chenzhu Xiang +3 more
wiley +1 more source
Anorectal Malformations: The Pivotal Role of the Good Clinical Practice
Anorectal malformations (ARM) without a fistula are a rare congenital condition. Although may seem more simple to repair compared with ARM with fistulas, surgery has proved to be challenging. We report the case of a newborn who presented a well‐formed anus and normal genitalia; a blind‐ending anal canal was detected after the insertion of a rectal ...
Filomena Valentina Paradiso +4 more
wiley +1 more source
Post‐operative colonic manometry in children with anorectal malformations: A systematic review
Abstract Background Children with anorectal malformations may experience constipation and fecal incontinence following repair. The contribution of altered anorectal function to these persistent symptoms is relatively intuitive; however, colonic motility in this cohort is less well understood.
Hannah M. E. Evans‐Barns +6 more
wiley +1 more source
Magnetic resonance imaging evaluation after anorectal pull-through surgery for anorectal malformations : a comprehensive review [PDF]
Anorectal malformations (ARM) include congenital anomalies of the distal anus and rectum with or without anomalies of the urogenital tract. Posterior sagittal anorectoplasty (PSARP) and minimally invasive laparoscopically assisted anorectal pull-through (
core +1 more source
Rare Associations with Posterior Urethral Valves
Posterior urethral valves are a common cause of congenital bladder outlet obstruction. Known associations include cardiac malformations and gastrointestinal abnormalities. In this case series, we report on two cases of PUV associated with anorectal malformations along with a case of PUV in monochorionic diamniotic twins.
Ahmed Osama Mohamed +4 more
wiley +1 more source

