| Literature DB >> 33136487 |
Fabrício Guimarães Gonçalves1, César Augusto Pinheiro Ferreira Alves1, Beth Heuer1, James Peterson1, Angela N Viaene1, Sara Reis Teixeira1, Juan Sebastián Martín-Saavedra1, Savvas Andronikou1, Amy Goldstein1, Arastoo Vossough1.
Abstract
Primary mitochondrial disorders (PMDs) constitute the most common cause of inborn errors of metabolism in children, and they frequently affect the central nervous system. Neuroimaging findings of PMDs are variable, ranging from unremarkable and nonspecific to florid and highly suggestive. An overview of PMDs, including a synopsis of the basic genetic concepts, main clinical symptoms, and neuropathologic features, is presented. In addition, eight of the most common PMDs that have a characteristic imaging phenotype in children are reviewed in detail. Online supplemental material is available for this article. ©RSNA, 2020.Entities:
Mesh:
Year: 2020 PMID: 33136487 DOI: 10.1148/rg.2020200052
Source DB: PubMed Journal: Radiographics ISSN: 0271-5333 Impact factor: 5.333