Sturge-Weber Syndrome

Below you will find more information about Sturge-Weber Syndrome from Medigest. If you believe that you are suffering from any of the symptoms of Sturge-Weber Syndrome it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Sturge-Weber Syndrome and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Sturge-Weber Syndrome comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Sturge-Weber syndrome, sometimes known as encephalotrigeminal angiomatosis, is an extremely rare congenital neurological and skin disorder.


In the "incomplete" forms of SWS, CNS angiomas arise without cutaneous features and therefore, no suspicion of SWS occurs until a seizure or other neurologic problem develops. Because of this, the diagnosis of SWS is not always straightforward.


Laser treatment may be administered to lighten or remove the birthmark. Anticonvulsant medications may be utilized to control seizures. Doctors recommend yearly monitoring for glaucoma, and surgery may be performed on more severe cases. Physical therapy should be considered for infants and children experiencing muscle weakness.

Symptoms and Signs

Sturge-Weber syndrome is characterized at birth by seizures accompanied by a large port-wine stain birthmark on the forehead and upper eyelid of one side of the face. The birthmark can differ in color from light pink to deep purple, and is caused by an overabundance of capillaries around the ophthalmic branch of the trigeminal nerve, just beneath the surface of the face.


Sturge-Weber syndrom is the result of residual embryonal blood vessels and their secondary effects on surrounding brain tissue.

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