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Urorectal septum malformation sequence in a newborn with vacterl association.
Author(s):
1. Soumya Patra: Department of Paediatric Medicine, NRS Medical College and Hospital Kolkata, India
2. Radheshyam Purkait: Department of Paediatric Medicine, NRS Medical College and Hospital Kolkata, India
Abstract:
Urorectal septum malformation sequence (URSMS) is an extremely rare anomaly, consists of multiple system anomalies including ambiguous genitalia, absence of a perineal opening, an imperforate anus, and urological, colonic and lumbosacral defects. We describe a newborn with characteristic URSMS who also had features of congenital varus deformity of leg, polydactyly, tracheo-oesophageal fistula, cardiac defect, anal atresia and hydronephrosis in antenatal ultrasound characteristic of VACTERL association.
Page(s): 116-117
DOI: DOI not available
Published: Journal: Journal of College of Physicians and Surgeons--Pakistan : JCPSP, Volume: 22, Issue: 2, Year: 2012
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