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Article

Refractory cerebral infarction in a child with an ACTA2 mutation.

Brain & development - 1 Apr 2021

Kanamori Keita, Sakaguchi Yuri, Tsuda Kyoji, Ihara Satoshi, Miyama Sahoko

Abstract excerpt

INTRODUCTIONS: A specific mutation in the ACTA2 gene is known to cause multisystemic smooth muscle dysfunction syndrome, which is associated with cerebrovascular diseases and various organ disorders. Cerebral infarctions resulting from severe vasculopathy can be refractory; however, there are no previous reports describing the detailed clinical course of recurrent cerebral infarctions due to an ACTA2 mutation....

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Identifiers

PMID: 33342581
DOI: 10.1016/j.braindev.2020.12.001

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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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