encephalotrigeminal angiomatosis , auch: encephalotrigeminal syndrome

Sturge-Weber syndrome, sometimes referred to as encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder.

He performed extensive studies of diseases involving the lacrimal apparatus, and in 1860 described the association of facial naevus flammeus with buphthalmos in a disease now known as encephalotrigeminal angiomatosis.

Dimitri Disease Encephalofacial Angiomatosis Encephalotrigeminal Angiomatosis Leptomeningeal Angiomatosis Meningeal Capillary Angiomatosis Sturge-Kalischer-Weber Syndrome Sturge-Weber Phakomatosis SWS None Sturge-Weber syndrome is composed of three major symptoms.