Sturge-Weber syndrome

Sturge-Weber syndrome, also known as encephalotrigeminal angiomatosis, is a rare congenital neurocutaneous syndrome involving vascular malformations of the skin, eyes, and brain. It is primarily characterized by angiomas affecting the leptomeninges, the facial area innervated by the trigeminal nerve, and the choroid of the eye. Onset typically occurs during infancy or early childhood, presenting with neurological and ocular symptoms.