RBS patients typically have limb malformations involving symmetric reduction in the number of digits, and the length or presence of bones in the arms and legs, but the severity of these abnormalities is quite variable, even within families [1].
The combination of hemisacrum, anorectal malformation (ARM), and presacral mass constitutes CS [ 9].
The aim of this study is to evaluate postoperatively bowel symptoms of antegrade colon enema through appendicostomies in preschool children with anorectal malformation (ARM).
Children with anorectal malformation (ARM) should be fecally clean when starting school, at the age of 5-6 years, in order to be socially accepted.
CS is a rare form of caudal regression syndrome (CRS), consisting in anorectal malformation (ARM), sacral bone deformity and presacral mass [ 9].
Anorectal malformations (ARM) are common congenital anomalies seen throughout the world.
Patients with anorectal malformations (ARM), Hirschsprung disease (HD), and colonic motility disorders often require care from specialists across a variety of fields, including colorectal surgery, urology, gynecology, and GI motility.
To compare MRI and colostography/fistulography in neonates with anorectal malformations (ARM), using surgery as reference standard.
This study was designed to investigate the expression of Notch-1 and Jagged-2 in the terminal hindgut in ethylenethiourea (ETU -exposed rat ETU -exposed anorattal malformations (ARMs) and its potembryosassociation with the manorectalmalformationserminARMsindgut in ands.
Anorectal malformations (ARMs) often result in lifelong problems with defecation.
Patients with anorectal malformations (ARMs) have a high incidence of genitourinary anomalies.
