Overview
Susac syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Research Evidence
Peer-reviewed studies linked via MeSH term "Syndrome, Susac" from the MEDLINE/PubMed database.
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Susac Syndrome: A Systematic Review and Survival Analysis.
[object Object], [object Object], [object Object] et al. · Clin Rev Allergy Immunol · 2025
PMID: 40715894Meta-Analysis
Clinical Characterization and Ancillary Tests in Susac Syndrome: A Systematic Review.
[object Object], [object Object], [object Object] et al. · Neurol Neuroimmunol Neuroinflamm · 2024
Bridging the triad: A comprehensive review of Susac's syndrome.
[object Object], [object Object] · J Neuroimmunol · 2025
PMID: 40857987Review
Susac Syndrome: A Multidisciplinary Approach to Diagnosis and Management with an Emphasis on Ophthalmic Involvement.
[object Object] · Semin Ophthalmol · 2025
PMID: 39576155Review
The neurocognitive and neuropsychiatric manifestations of Susac syndrome: a brief review of the literature and future directions.
[object Object], [object Object], [object Object] et al. · Neurol Sci · 2024
Rare primary vasculitis: update on multiple complex diseases and the new kids on the block.
[object Object], [object Object], [object Object] et al. · Adv Rheumatol · 2024
PMID: 39385260Review
Susac syndrome and pregnancy: a relationship to clarify. About two cases and review of the literature.
[object Object], [object Object], [object Object] et al. · J Matern Fetal Neonatal Med · 2022
PMID: 31937158Review
Susac syndrome: challenges in the diagnosis and treatment.
[object Object], [object Object], [object Object] · Brain · 2022
PMID: 35136969Review
Fundamental mechanistic insights from rare but paradigmatic neuroimmunological diseases.
[object Object], [object Object], [object Object] et al. · Nat Rev Neurol · 2021
PMID: 34050331Review
Headache in Susac's Syndrome.
[object Object], [object Object] · Curr Pain Headache Rep · 2021
PMID: 33738651Review
Search all PubMed articles for Susac syndrome
Research data from MEDLINE/PubMed
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Headache
Very frequent (80-99%)HP:0002315
Cognitive deficits
Frequent (30-79%)HP:0100543
Confusion
Frequent (30-79%)HP:0001289
Corpus callosum abnormality
Frequent (30-79%)HP:0001273
Generalised decreased muscle tone
Frequent (30-79%)HP:0001290
Sensorineural deafness
Frequent (30-79%)HP:0000407
Visual loss
Frequent (30-79%)HP:0000572
Abnormal emotion processing
Occasional (5-29%)HP:0100851
Behavioural/Psychiatric abnormality
Occasional (5-29%)HP:0000708
Difficulty articulating speech
Occasional (5-29%)HP:0001260
Dizziness
Occasional (5-29%)HP:0002321
Double vision
Occasional (5-29%)HP:0000651
Dullness
Occasional (5-29%)HP:0001254
Eye movement issue
Occasional (5-29%)HP:0000496
Inability to coordinate movements when walking
Occasional (5-29%)HP:0002066
Lack of feeling, emotion, interest
Occasional (5-29%)HP:0000741
Muscle weakness
Occasional (5-29%)HP:0001324
Nausea and vomiting
Occasional (5-29%)HP:0002017
Personality changes
Occasional (5-29%)HP:0000751
Psychosis
Occasional (5-29%)HP:0000709
Pyramidal tract dysfunction
Occasional (5-29%)HP:0002493
Ringing in ears
Occasional (5-29%)HP:0000360
Sensory impairment
Occasional (5-29%)HP:0003474
Related Conditions
Quick Facts
- SNOMED CT
- 702575003
- UMLS CUI
- C2717757
- Fully Specified Name
- Retinocochleocerebral vasculopathy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 23
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.