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Up to: Hereditary neurological disease · Eye disorder · Neurocutaneous syndrome

Sturge-Weber syndrome

Sturge-Weber syndrome (SWS) is a rare congenital neurocutaneous disorder characterized by facial capillary malformations and/or cerebral and ocular ipsilateral vascular malformations that result in variable degrees of ocular and neurological anomalies.

8 trials tagged with this condition →

This condition has no sub-types.