Sturge-Weber Syndrome

Category:
Neurological Disorder

Prevalence:
In The US: About 1 in 20,000.

Also Called:
Encephelotrigeminal Angiomatosis

Resources:
U.S. National Library of Medicine

WebMD

 

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Sturge-Weber syndrome is a neurological disorder indicated at birth by a port-wine stain birthmark on the forehead and upper eyelid of one side of the face. The birthmark can vary in color from light pink to deep purple and is caused by an overabundance of capillaries around the trigeminal nerve just beneath the surface of the face. Sturge-Weber syndrome is also accompanied by abnormal blood vessels on the brain surface and the loss of nerve cells and calcification of underlying tissue in the cerebral cortex of the brain on the same side of the brain as the birthmark. Neurological symptoms include seizures that begin in infancy and may worsen with age. Convulsions usually happen on the side of the body opposite the birthmark and vary in severity. There may be intermittent or permanent muscle weakness on the same side. Some children will have developmental delays and cognitive impairment; most will have glaucoma (increased pressure within the eye) at birth or developing later. The increased pressure within the eye can cause the eyeball to enlarge and bulge out of its socket (buphthalmos). There is an increased risk for migraine headaches. Sturge-Weber syndrome rarely affects other body organs.

Sturge-Weber Syndrome In The News

21month Old Baby Boy from Uganda Suffering from Rare Sturge-Weber Syndrome Walks Tall After Cell Based Therapy in Mumbai

Read More    published: 10/16/2018

Corina’s Story: Adopting a Child with Sturge-Weber Syndrome

Read More    published: 05/01/2015

Ophthalmic Alterations in the Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome, and the Phakomatosis Pigmentovascularis: An Independent Group of Conditions?

Read More    published: 04/27/2015

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