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An instance of syringomyelia that is caused by an inherited modification of the individual's genome.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for familial syringomyelia.
10 publications have been identified in PubMed for familial syringomyelia. Research spans Review / Meta-Analysis (50%), Case Report / Case Series (30%), and Epidemiology / Natural History (20%).
Research Type | Count | % of Total |
|---|---|---|
Research summaries | 5 | 50% |
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 1:55 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
3 |
30% |
Disease patterns and progression | 2 | 20% |
Rosdi SNM (2025). [PMID: 40047162](https://pubmed.ncbi.nlm.nih.gov/40047162/). *Croat Med J*. [Case Report / Case Series]
Yamamoto FK (2025). [PMID: 40266040](https://pubmed.ncbi.nlm.nih.gov/40266040/). *Einstein (Sao Paulo)*. [Case Report / Case Series]
Mekbib KY (2025). [PMID: 40315599](https://pubmed.ncbi.nlm.nih.gov/40315599/). *J Neurosurg Pediatr*. [Epidemiology / Natural History]
Jones R (2025). [PMID: 40065427](https://pubmed.ncbi.nlm.nih.gov/40065427/). *Fluids Barriers CNS*. [Review / Meta-Analysis]
Kiran VR (2024). [PMID: 39524280](https://pubmed.ncbi.nlm.nih.gov/39524280/). *J Orthop Case Rep*. [Case Report / Case Series]
Zhang W (2024). [PMID: 39435986](https://pubmed.ncbi.nlm.nih.gov/39435986/). *CNS Neurosci Ther*. [Review / Meta-Analysis]
Visocchi M (2024). [PMID: 39452020](https://pubmed.ncbi.nlm.nih.gov/39452020/). *Brain Sci*. [Review / Meta-Analysis]
Dhawan A (2024). [PMID: 38608294](https://pubmed.ncbi.nlm.nih.gov/38608294/). *J Neurosurg Spine*. [Review / Meta-Analysis]
Shaibani A (2024). [PMID: 39461769](https://pubmed.ncbi.nlm.nih.gov/39461769/). *Neuroimaging Clin N Am*. [Review / Meta-Analysis]
Beers BG (2024). [PMID: 39255206](https://pubmed.ncbi.nlm.nih.gov/39255206/). *J Zoo Wildl Med*. [Epidemiology / Natural History]