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De Novo Development of Moyamoya Disease after Stereotactic Radiosurgery for Brain Arteriovenous Malformation in a Patient With RNF213 p.Arg4810Lys (rs112735431).

World neurosurgery - 1 Aug 2020

Torazawa Seiei, Miyawaki Satoru, Shinya Yuki, Kawashima Mariko, Hasegawa Hirotaka, Dofuku Shogo, Uchikawa Hiroki, Kin Taichi, Shin Masahiro, Nakatomi Hirofumi, Saito Nobuhito

Abstract excerpt

BACKGROUND: Reports of cases diagnosed as Moyamoya disease (MMD) after stereotactic radiosurgery (SRS) for arteriovenous malformation (AVM) are extremely rare. In recent years, ring finger protein 213 (RNF213) has been identified as a susceptibility gene of MMD, but the mechanism by which MMD develops remains unclear. Those cases of de novo development of MMD may provide some clues to clarify the mechanism of...

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PMID: 32434013
DOI: 10.1016/j.wneu.2020.05.068

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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