Congenital anal atresia with rectovestibular fistula scoliosis unilateral renal agenesis and finger defect (VACTERL association) in a patient with partial bicornuate uterus and distal vaginal atresia

摘要

Rationale:Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect (VACTERL) association and Müllerian duct anomalies are rare conditions. We present a rare condition with the co-occurrence of the VACTERL association and Müllerian duct hypoplasia to characterize patients’ clinical presentations, outcomes, and treatment.