Abstract
Sturge-Weber syndrome (SWS) is a rare, neurocutaneous syndrome associated with port-wine stains of the face, glaucoma, leptomeningeal angiomas, seizures, and intellectual disability. Few studies report an overall description of findings and treatment for children with Sturge-Weber glaucoma (SWG), which can be challenging to manage.
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Schedule a callMore From: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
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