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sturge-weber syndrome

sturge-weber syndrome in Medicine

Sturge-Weber syndrome Sturge-Web·er syndrome (stûrj'wěb'ər)
n.
A congenital syndrome characterized by a port-wine stain nevus in the distribution of the trigeminal nerve, homolateral meningeal angioma with intracranial calcification and neurologic signs, and angioma of the choroid, often with secondary glaucoma. Also called angiophacomatosis, encephalofacial angiomatosis, encephalotrigeminal angiomatosis, Sturge's disease, Sturge-Weber disease.

The American Heritage® Stedman's Medical Dictionary
Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.
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