Nonsurgical treatment of cerebral ischemia associated with ACTA2 cerebral arteriopathy: a case report and literature review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00381-021-05360-z.pdf
Reference19 articles.
1. Lu H, Fagnant PM, Krementsova EB, Trybus KM (2016) Severe molecular defects exhibited by the R179H mutation in human vascular smooth muscle α-actin*. J Biol Chem 291(41):21729–21739
2. Milewicz DM, Østergaard JR, Ala-Kokko LM et al (2010) De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction. Am J Med Genet A 152A(10):2437–2443
3. Munot P, Saunders DE, Milewicz DM et al (2012) A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations. Brain 135(8):2506–2514
4. Regalado ES, Mellor-Crummey L, Backer JD et al (2018) Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations. Genet Med 20(10):1206–1215
5. Rutledge WC, Choudhri O, Walcott BP, Benet A, Fox CK, Gupta N, Lawton MT (2016) Indirect and direct revascularization of ACTA2 cerebral arteriopathy: feasibility of the superficial temporal artery to anterior cerebral artery bypass with posterior auricular artery interposition graft: case report. J Neurosurg Pediatrics 18(3):339–343
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