Brain MRI phenotype of ACTA2 mutation illustrated in Eurorad teaching case

New Eurorad teaching case demonstrates the distinctive neuroradiological features of ACTA2 mutations, which cause smooth muscle dysfunction syndrome with characteristic brain MRI findings.

• Teaching case from ESR's Eurorad highlights typical imaging findings of ACTA2 mutation.
• Aids radiologists in recognizing this rare genetic condition on brain MRI.
• Intended for radiology trainees and neuroradiologists.

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