{Reference Type}: Case Reports
{Title}: Undiagnosed Epileptic Case Since Childhood of Sturge-Weber Syndrome: First Case Report from Somalia.
{Author}: Mohamed SA;Sidow NO;Adam BA;Hassan MS;Ibrahim AA;Osman MF;Ahmed A;Roble AA;
{Journal}: Int Med Case Rep J
{Volume}: 17
{Issue}: 0
{Year}: 2024
暂无{DOI}: 10.2147/IMCRJ.S463858
{Abstract}: Sturge-Weber syndrome is a rare, sporadic, progressive neurocutaneous condition that presents with congenital hamartomatous malformations, epilepsy, and a variety of facial symptoms. We discussed a rare case of an eighteen-year-old female child who came to our neurology department with status epilepticus, mental impairment, and a port-wine in the lateral left side of her face. We diagnosed Sturge-Weber syndrome after a thorough neurological and radiological evaluation. The purpose of presenting this case is to illustrate both the characteristic presentation and the complications associated with managing Sturge-Weber syndrome.