Titlebook: Anorectal Malformations in Children; Embryology, Diagnosi Alexander M. Hohlschneider,John M. Hustson Book 20061st edition Springer-Verlag B

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Congenital Pouch Colonn anomaly in which all or part of the colon is replaced by a pouch-like dilatation, which communicates distally with the urogenital tract via a large fistula. In this condition, a supralevator anorectal malformation (ARM) is associated with a colonic pouch of variable size (5–15 cm in diameter). The

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Rectal Atresia and Rectal Ectasiam the southern part of India at one stage. The anomaly is no longer as common, even in that region. The male:female ratio is 7:3. In fact, because of its rarity, many pediatric surgeons have not had the chance to see and manage such cases. Rectal atresia is characterized by the presence of the proxi

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Rare/Regional Variantsine the border between the rare and the not-so-rare. As far as anorectal malformations (ARM) are concerned, the problem is compounded by the vagaries of space and time. Lesions that are nonexistent or super-rarities in one part of the world are common in another part. Lesions that were common at one

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Nonurologic Anomalies Associated with Anorectal Malformationstions, it is surprising that more patients with anorectal malformations (ARM) and esophageal atresia/tracheoesophageal fistula (EA/TEF) do not manifest both anomalies. The collections of data over the years have indicated that the coincidence of the major associated anomalies has remained remarkably

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Urological Problems in Children with Anorectal Malformationssized. This is surprising as the association between urological anomalies and ARM is well described and is a known feature of both the VATER (acronym of Vertebral and vascular anomalies, Anal atresia, Tracheoesophageal fistula, Esophageal atresia, and Renal anomalies, Radial dysplasia) and VACTERL (

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