INFORMATION ON ENCEPHALOTRIGEMINAL ANGIOMATOSIS

Encephalotrigeminal Angiomatosis (Sturge-Weber syndrome) is a uncommon disorder present at birth. It is characterized by a birthmark, generally on the face, known as a port wine stain (from too many blood vessels just under the skin) and neurologic problems.

CAUSES OF ENCEPHALOTRIGEMINAL ANGIOMATOSIS

The cause of Encephalotrigeminal Angiomatosis is unknown. There is no known hereditary component

SYMPTOMS OF ENCEPHALOTRIGEMINAL ANGIOMATOSIS

• Port-wine stain (more ordinary on the face than the body)
• Convulsions
• Paralysis or weakness on one side
• Glaucoma
• Learning disabilities

TREATMENT OF ENCEPHALOTRIGEMINAL ANGIOMATOSIS

Treatment is based on the patient's signs and symptoms:
• Anticonvulsant medicine for convulsions.
• Physical therapy for paralysis or weakness
• Eye drops or surgery for glaucoma
• Laser therapy for port wine stains