Sturge-Weber syndrome
MONDO:0008501Sturge-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.
Also known as: SWS, Sturge Weber Syndrome, Sturge Weber syndrome, Sturge-Weber disease, Sturge-Weber syndrome, Sturge-Weber syndrome, somatic, mosaic, Sturge-Weber-Dimitri syndrome, Sturge-Weber-Krabbe angiomatosis
15 clinical trials for this condition and its sub-types.
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20-Year study tests precision medicine for rare Brain-Skin disorders
Knowledge-focused CompletedThis completed study looked at 1,200 people with neurocutaneous syndromes (NF1, TSC, SWS, VHL) in Western China. Researchers compared those who received genetic testing, targeted drugs, and coordinated specialist care against those who got standard care. The goal was to see if pr…
Sponsor: West China Hospital • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:09 UTC
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French study tracks port wine stains in kids to uncover hidden risks
Knowledge-focused CompletedThis study followed 150 children aged 2 to 12 who have a port wine stain on a leg. Researchers tracked how the stain changes as the child grows, and whether it leads to problems like blood vessel issues or bone growth differences. The goal was to learn more about the condition an…
Phase: NA • Sponsor: University Hospital, Tours • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:06 UTC