Results 51 to 60 of about 586,789 (263)
Background/purpose Surgical management of high-type anorectal malformations (ARM) has evolved over the years with the widespread of the laparoscopic approach over the last two decades.
Mohammad Anas AlShawa+2 more
doaj +1 more source
Anorectal malformation and Hirschsprung disease in an otherwise healthy infant
Background: Hirschsprung disease and anorectal malformations are two conditions that are rarely associated with one another. Current reports of anorectal malformations with concurrent Hirschsprung disease predominantly describe children with genetic ...
Audra Rougraff+2 more
doaj
Anomalias da inervação do trato digestório de fetos de ratas expostas à etilenotioureia [PDF]
PURPOSE: The pathophysiology of abnormalities associated with myenteric plexus lesions remains imperfectly understood. Such abnormalities have been correlated with subocclusive intestinal conditions in children with Hirschsprung's disease, cases of ...
Lemos, Patrícia Veruska Ribeiro Barbosa+5 more
core +3 more sources
European consensus meeting of ARM-Net members concerning diagnosis and early management of newborns with anorectal malformations. [PDF]
The ARM-Net (anorectal malformation network) consortium held a consensus meeting in which the classification of ARM and preoperative workup were evaluated with the aim of improving monitoring of treatment and outcome.
A Bischoff+30 more
core +3 more sources
Involvement of the HLXB9 homeobox gene in Currarino syndrome [2] [PDF]
published_or_final_versio
Belloni, E+9 more
core +2 more sources
Genome-wide copy number variation study in anorectal malformations [PDF]
Anorectal malformations (ARMs, congenital obstruction of the anal opening) are among the most common birth defects requiring surgical treatment (2-5/10 000 live-births) and carry significant chronic morbidity.
Baum, L+36 more
core +1 more source
The long‐term anorectal outcomes of non‐surgically treated patients diagnosed with minor types of ARM seem optimal. Most of these patients experience no constipation or fecal incontinence; some experience constipation and relatively seldom fecal incontinence. Furthermore, most patients possess all the known fecal continence mechanisms.
Venla E. C. den Hollander+3 more
wiley +1 more source
Is a low sacral ratio associated with primary vesicoureteral reflux in children? [PDF]
Introduction: The association of sacral anomalies with fecal incontinence and lower urinary tract dysfunction is known. The sacral ratio is proposed as a tool for evaluation of sacral development. The aim of this cross-sectional study was to evaluate the
Esfahani, S.T.+2 more
core
ABSTRACT Objective This systematic review and meta‐analysis compare the outcomes of primary laryngotracheal reconstruction (LTR) and partial cricotracheal resection (PCTR) in managing moderate‐grade pediatric subglottic stenosis (severe Grade II and Grade III).
Bigyan Raj Gyawali+8 more
wiley +1 more source
Myelodysplasia in children with anorectal malformations [PDF]
Objective: To compare computed tomography and magneticresonance imaging accuracy to diagnose myelodysplasia inpatients with anorectal anomaly, to verify the prevalence of tetheredspinal cord, and to investigate if there is a direct relation betweenthe ...
Karine Furtado Meyer+2 more
doaj