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Rare RNF213 variant in adolescent with moyamoya disease.

I Cardoso1, M Pinto1, A Araújo1

  • 1Centro Hospitalar de Vila Nova de Gaia, Vila Nova de Gaia, Portugal.

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|February 27, 2023
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Summary
This summary is machine-generated.

Moyamoya disease, a progressive steno-occlusive condition, is linked to RNF213 gene variants. A case report details a European patient with the c.12185G>A, p.(Arg4062Gln) variant, previously found in Asian populations.

Area of Science:

  • Genetics
  • Neurology
  • Vascular Medicine

Background:

  • Moyamoya disease is a progressive steno-occlusive condition affecting major intracranial arteries.

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  • It increases the risk of stroke, cognitive impairment, and developmental delays.
  • The RNF213 gene is a key susceptibility gene, with the p.R4810K variant found in 95% of familial cases.