Case Report
Sai Sampath Kumar, Ravi Kiran,
Abstract
Colpocephaly is an abnormal enlargement of the occipital horn of the lateral ventricle, also described as persistence of the fetal configuration of the lateral ventricles. Since it was first described, colpocephaly has been found in association with several abnormalities of the brain. Various etiologies have been postulated, including intrauterine/perinatal injuries, genetic disorders, and an error of morphogenesis. We report a case of colpocephaly associated with absence of splenium of the corpus callosum presented with neurodevelopmental delay and epilepsy.