A CASE REPORT OF STURGE WEBER SYNDROME

The Sturge-Weber Syndrome, also known as encephalotrigeminal angiomatosis, is a rare vascular neurocutaneous alteration. It is characterized by facial nevus, seizures, hemiparesis, intracranial calcification and mental retardation. Here we report a case of Sturge-Weber syndrome who presented with a cutaneous vascular nevus on the face during childhood as well as epileptic crisis episodes