Caudal Regression Syndrome is characterized by malformed genitals, anal atresia, and kidney abnormalities due to absent sacral vertebrae. It occurs in approximately 1 in 7,500 births and 16% of cases involve children of diabetic mothers. Imaging shows conus abnormalities in 95% of symptomatic patients, such as a truncated or high-lying spinal cord tip with a sparse cauda equina nerve bundle. There are two types - one with a truncated and high cord, and another with a truncated cord that is inferiorly located and tethered.