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Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for magic syndrome.
8 publications have been identified in PubMed for magic syndrome. Research spans Case Report / Case Series (63%), Other (25%), and Clinical Trial Publication (13%).
Klepper J (2026). [PMID: 41830506](https://pubmed.ncbi.nlm.nih.gov/41830506/). *Epilepsia Open*. [Case Report / Case Series]
Chiu MZ (2026). [PMID: 41151493](https://pubmed.ncbi.nlm.nih.gov/41151493/). *Surgery*. [Clinical Trial Publication]
Cao Y (2025). [PMID: 40979852](https://pubmed.ncbi.nlm.nih.gov/40979852/). *Clin Nephrol Case Stud*. [Case Report / Case Series]
Suzuki T (2025). [PMID: 40584762](https://pubmed.ncbi.nlm.nih.gov/40584762/). *J Rheum Dis*. [Case Report / Case Series]
Touma E (2025). [PMID: 41241395](https://pubmed.ncbi.nlm.nih.gov/41241395/). *J Rheumatol*. [Other]
Arvind MN (2025). [PMID: 40553604](https://pubmed.ncbi.nlm.nih.gov/40553604/). *J Assoc Physicians India*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 12:10 AM UTC
Patient Advocacy Groups (PAGs) provide support, resources, and community for patients and caregivers.
European rare disease database
Genetic and Rare Diseases Info Center
Schifter M (2025). [PMID: 40223546](https://pubmed.ncbi.nlm.nih.gov/40223546/). *Med J Aust*. [Other]
Lin M (2024). [PMID: 39543079](https://pubmed.ncbi.nlm.nih.gov/39543079/). *Med J Aust*. [Case Report / Case Series]