The aim of the study was to study the case of a three-year-old girl with Sturge-Weber Syndrome without Facial Nevus. Initially, the baby was diagnosed with epilepsy after repeated seizures that began at the age of three months. The study came to a number of conclusions, the most important of which is that SWS syndrome is classified into three types: the first type includes the skin, eye and brain, in the second type the brain is not affected, and in the third type only the brain is affected, and that the occurrence of SWS without facial nevus is unknown. The study came up with several recommendations, the most important of which is the need for surgical consideration in patients with drug-resistant epilepsy.