Encephalotrigeminal Angiomatosis, also called Sturge-Weber syndrome, is a congenital disorder characterised by a vascular birthmark and neurological abnormalities. This disorder may include eye and ...

There is no cure, but it is not fatal. Other names include encephalotrigeminal angiomatosis, encephalofacial angiomatosis, or Sturge-Weber-Dimitri syndrome. A person who has Sturge-Weber syndrome ...

The medical term for SWS is encephalotrigeminal angiomatosis, according to the National Organization for Rare Disorders, SWS occurs in one of every estimated 20,000 to 50,000 live births.