Sturge–Weber syndrome
ICD-10: Q85.8MeSH: D013341ORPHA: 3205
Overview
neurological and skin disorder associated with port-wine stains of the face, glaucoma, seizures, intellectual disability, and cerebral malformations
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with Sturge–Weber syndrome, sourced from HPO and Orphanet clinical annotations.
HyperostosisOcular painFacial capillary hemangiomaSeizureCapillary hemangiomaStrabismusGlaucomaOptic atrophyAtypical behaviorDelayed speech and language developmentVisual field defectIntellectual disabilityStrokeHyperreflexiaHeadacheAttention deficit hyperactivity disorderLens luxationArachnoid hemangiomatosisInfantile spasmsNeurodevelopmental delayAbnormal cerebral vascular morphologyGingival overgrowthHydrocephalusMacrocephalyHearing abnormalityAbnormality of visionConjunctival telangiectasiaRetinal detachmentBuphthalmosVisual lossAbnormal choroid morphologyIris colobomaBlindnessDental malocclusionAutistic behaviorHeterochromia iridisCorneal dystrophyDysphagiaCerebral cortical atrophyPulmonary embolismChiari malformationSleep disturbanceCerebral calcificationVenous thrombosisChoroidal hemangiomaAbnormal retinal vascular morphologyEpiphoraCentral hypothyroidismHemianopiaReduced circulating growth hormone concentrationVisceral angiomatosis
Classification & Codes
ICD-10 Code
Q85.8MeSH Code
D013341Orphanet Code
ORPHA:3205Sturge–Weber syndrome
| ICD-10 | Q85.8 |
| MeSH | D013341 |
| Orphanet | ORPHA:3205 |
| Treatments | 0 drug(s) |
| Symptoms on record | 51 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO