Overview
Leukoencephalopathy is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Research Evidence
Peer-reviewed studies linked via MeSH term "Leukoencephalopathies" from the MEDLINE/PubMed database.
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Phenotyping mitochondrial glutamyl-tRNA synthetase deficiency (EARS2): A case series and systematic literature review.
[object Object], [object Object], [object Object] et al. · Neurobiol Dis · 2024
PMID: 39173847Meta-Analysis
The Dark side of the White Matter. Diffuse subcortical White Matter Hypointensity on T2/FLAIR: A systematic review of a frequently underrecognized sign.
[object Object], [object Object], [object Object] et al. · J Neurol Sci · 2024
PMID: 38224629Meta-Analysis
Symmetric leukoencephalopathy associated with systemic lupus erythematosus: A systematic review of a distinctive neurorheumatologic syndrome.
[object Object], [object Object], [object Object] et al. · Mult Scler Relat Disord · 2024
PMID: 38943754Meta-Analysis
Brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS): new cases, systematic literature review, and associations with CSF1R-ALSP.
[object Object], [object Object], [object Object] et al. · Orphanet J Rare Dis · 2023
Neuroimaging phenotypes of CSF1R-related leukoencephalopathy: Systematic review, meta-analysis, and imaging recommendations.
[object Object], [object Object], [object Object] et al. · J Intern Med · 2022
PMID: 34875121Meta-Analysis
Association Between Small Vessel Disease Markers, Medial Temporal Lobe Atrophy and Cognitive Impairment After Stroke: A Systematic Review and Meta-Analysis.
[object Object], [object Object], [object Object] et al. · J Stroke Cerebrovasc Dis · 2021
PMID: 33227579Meta-Analysis
One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family.
[object Object], [object Object], [object Object] et al. · J Stroke Cerebrovasc Dis · 2021
PMID: 34303089Meta-Analysis
The relation between antihypertensive treatment and progression of cerebral small vessel disease: A systematic review and meta-analysis of randomized controlled trials.
[object Object], [object Object], [object Object] et al. · Medicine (Baltimore) · 2021
Age and Diastolic Blood Pressure Play an Important Role in the Progression of White Matter Lesions: A Meta-Analysis.
[object Object], [object Object], [object Object] et al. · Eur Neurol · 2020
PMID: 32906133Meta-Analysis
Brain abnormalities in COVID-19 acute/subacute phase: A rapid systematic review.
[object Object], [object Object], [object Object] · Brain Behav Immun · 2020
Search all PubMed articles for Leukoencephalopathy
Research data from MEDLINE/PubMed
Related Conditions
Acute hemorrhagic leukoencephalitis(child)
Posterior reversible encephalopathy syndrome(child)
Presenile dementia with bone cysts(child)
HCC - hypomyelination and congenital cataract(child)
Hereditary diffuse leukoencephalopathy with axonal spheroids(child)
Infantile leukoencephalopathy and megalencephaly(child)
Mitochondrial neurogastrointestinal encephalomyopathy syndrome(child)
Progressive cavitating leukoencephalopathy(child)
Leukoencephalopathy co-occurrent with bilateral anterior temporal lobe cysts(child)
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome(child)
Cystic leukoencephalopathy without megalencephaly(child)
White matter disorder caused by infection(child)
Toxic white matter disorder(child)
White matter disorder co-occurrent and due to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy(child)
Leukoencephalopathy, dystonia, motor neuropathy syndrome(child)
Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation syndrome(child)
White matter disorder due to vascular abnormality(child)
White matter disorder due to vitamin B12 deficiency(child)
COXPD12 - combined oxidative phosphorylation defect type 12(child)
Leukoencephalopathy with mild cerebellar ataxia and white matter edema(child)
Quick Facts
- SNOMED CT
- 22811006
- UMLS CUI
- C0270612
- Fully Specified Name
- Leukoencephalopathy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.