Stable Leukoencephalopathy in a Patient With ACTA2-Associated Multisystem Smooth Muscle Disorder

Neurology. 2022 Aug 23;99(8):338-340. doi: 10.1212/WNL.0000000000200961. Epub 2022 Jun 17.

Authors

David Bieber¹, John D Port¹, Deborah L Renaud²

Affiliations

¹ From the Epilepsy Center (D.B.), Ann & Robert H. Lurie Children's Hospital of Chicago, IL; Departments of Radiology (J.D.P.), Neurology (D.L.R.), and Pediatrics (D.L.R.), Mayo Clinic, Rochester, MN.
² From the Epilepsy Center (D.B.), Ann & Robert H. Lurie Children's Hospital of Chicago, IL; Departments of Radiology (J.D.P.), Neurology (D.L.R.), and Pediatrics (D.L.R.), Mayo Clinic, Rochester, MN. [email protected].

PMID: 35715202
DOI: 10.1212/WNL.0000000000200961

No abstract available

Publication types

Case Reports

MeSH terms

Actins / genetics
Humans
Leukoencephalopathies* / diagnostic imaging
Leukoencephalopathies* / genetics
Muscle, Smooth
Muscular Diseases*
Mutation

Substances

ACTA2 protein, human
Actins