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Article

Intracranial Vessel Stenosis in a Young Patient with an MYH11 Mutation: A Case Report and Review of 2 Prior Cases.

World neurosurgery - 1 May 2020

Larson Anthony, Rinaldo Lorenzo, Brinjikji Waleed, Klaas James, Lanzino Giuseppe

Abstract excerpt

BACKGROUND: The MYH11 gene codes for smooth muscle myosin heavy chain, which has a critical function in maintaining vascular wall stability. Patients with this mutation most commonly have aortic and cardiac defects. Documented involvement of intracranial vessels is exceptional. CASE DESCRIPTION: A 29-year-old woman with a history of patent ductus arteriosus and aortic dissection was found to have incidental...

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Source

Identifiers

PMID: 32081817
DOI: 10.1016/j.wneu.2020.02.054

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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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