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biological

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Sturge–Weber syndrome

Sturge–Weber syndrome Sturge–Weber syndrome is a congenital condition that is not inherited and involves abnormal blood vessels and neurological changes.

Sturge–Weber syndrome is a congenital condition that is not inherited and involves abnormal blood vessels and neurological changes. It is marked by a facial port-wine stain and abnormal capillaries in the brain coverings and eye, and it can be associated with epilepsy, cognitive impairment, glaucoma, and vision problems.