Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy

ORPHA: 199354

Contents

1. Overview
2. Available Treatments
3. Clinical Presentation
4. Classification & Codes

Overview

medical condition

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 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy, sourced from HPO and Orphanet clinical annotations.

Atypical behaviorSpasticityGait disturbanceStroke-like episodeSpastic ataxiaArteriosclerosisBack painPseudobulbar paralysisCervical spondylosisLower limb painDeep cerebral white matter hyperintensitiesLocalized osteoporosisCognitive impairmentEmotional labilityAggressive behaviorDementiaIrritabilityApathyMental deteriorationHemiparesisStrokeRigidityAlopecia of scalpDiffuse cerebral atrophySomatic sensory dysfunctionAbnormal pyramidal signAbuliaAkinetic mutismNeck painBilateral tonic-clonic seizureKyphoscoliosis

Classification & Codes

Orphanet Code

ORPHA:199354

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy

Orphanet	`ORPHA:199354`
Treatments	0 drug(s)
Symptoms on record	31 signs
Status	published

Factual Authority

Last Updated3/20/2026

Clinical DataHPO · Orphanet

Drug DataFDA · EMA · CDSCO