Sneddon syndrome
ICD-10: M30.8MeSH: D018860ORPHA: 8202 Treatments Available
Overview
form of arteriopathy
Available Treatments (2)
Clinical Presentation
Signs and symptoms associated with Sneddon syndrome, sourced from HPO and Orphanet clinical annotations.
Atypical behaviorCutis marmorataThromboembolic strokeMigraineCerebral cortical atrophyHeadacheVertigoMemory impairmentSensorimotor neuropathyVascular skin abnormalityArterial stenosisDementiaHypertensionVisual field defectMental deteriorationHemiparesisMotor delayMuscle weaknessMitral regurgitationAortic regurgitationTransient ischemic attackDevelopmental regressionFocal-onset seizureImpaired visuospatial constructive cognitionLibman-Sacks lesionsDecreased glomerular filtration rateCerebral infarctDiminished ability to concentrateCognitive impairmentAmaurosis fugaxProteinuriaNephropathyDepressionSeizureTremorBicuspid aortic valveChoreaIntracranial hemorrhageAphasiaAntiphospholipid antibody positivityChilblainsPeripheral neuropathyOculomotor nerve palsyCentral retinal vein occlusionCentral retinal artery occlusionInternuclear ophthalmoplegiaRaynaud phenomenonCutaneous necrosisCerebral visual impairmentSuicide behaviorsSplinter hemorrhagesSubarachnoid hemorrhageIntraventricular hemorrhageLivedo racemosaInflammation
Classification & Codes
ICD-10 Code
M30.8MeSH Code
D018860Orphanet Code
ORPHA:820