医学
神经影像学
中枢神经系统
粒线体疾病
神经科学
儿科
精神科
线粒体DNA
内科学
遗传学
生物
基因
作者
Fabrício Guimarães Gonçalves,Cesar Alves,Beth Heuer,James T. Peterson,Angela N. Viaene,Sara Reis Teixeira,Juan Sebastián Martín-Saavedra,Savvas Andronikou,Amy Goldstein,Arastoo Vossough
出处
期刊:Radiographics
[Radiological Society of North America]
日期:2020-11-01
卷期号:40 (7): 2042-2067
被引量:36
标识
DOI:10.1148/rg.2020200052
摘要
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.
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