Although renal and cardiac malformations are commonly seen in Turner syndrome (TS), anorectal malformations, multicystic dysplastic kidney and interrupted aortic arch are quite rare in TS. A newborn with TS with three quite rare congenital malformations (imperforate anus/anal atresia associated with rectovestibular fistula, interrupted aortic arch, and multicystic dysplastic kidney) is presented.

PSARP is currently the most widely-used surgical technique for surgical correction of high and intermediary anorectal malformations, but there is much controversy in the literature about the postoperative evaluation of these cases. We studied 27 cases of anorectal malformations operated with PSARP from clinical and manometric aspects in order to analyze: 1) fecal continence; 2) the relationship...

In 68 patients with anorectal malformations cardiovascular anomalies (CVA) were seen in 15 and genitourinary (GU) anomalies in 30. CVA were more frequent (33%) whenever there was a GU anomaly. Ventricular septal defect was the most frequent lesion. All but 1 CVA occurred with type III anorectal malformation. The complexity of the cardiac lesion did not parallel that of the GU anomaly.

Diphallia is a very rare congenital anomalies occurs 1: 5-6 Million live birth. Associated like imperforate anus, vertebral deformities, double bladder, exstrophy of the cloacae, and duplication recto sigmoid may in association with this. Amongst all anorectal malformations common anomaly that can occur diphallia. Here we are presenting neonate functional penis, partial scrotal dysraphism, high...

The aim of this review article is to review the technique of laparoscopic assisted anorectoplasty (LAARP), its modifications, indications, contraindications and outcomes for anorectal malformations (ARM). LAARP was first introduced by Willital in 1998 and developed by Georgeson in 2000. Many modifications have taken place to reduce complications and to provide better functional outcomes. Recto-...