Literature DB >> 33136487

Primary Mitochondrial Disorders of the Pediatric Central Nervous System: Neuroimaging Findings.

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.

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Year:  2020        PMID: 33136487     DOI: 10.1148/rg.2020200052

Source DB:  PubMed          Journal:  Radiographics        ISSN: 0271-5333            Impact factor:   5.333


  5 in total

1.  Extended spinal cord involvement in adult-onset Leigh syndrome due to mitochondrial 10197G > A mutation.

Authors:  Yanping Wei; Min Qian; Yingmai Yang
Journal:  Neurol Sci       Date:  2022-07-31       Impact factor: 3.830

2.  Inherited neurometabolic diseases and the importance of imaging-based classification systems.

Authors:  Nina Ventura
Journal:  Radiol Bras       Date:  2022 May-Jun

3.  A child with mitochondrial DNA deletion presenting diabetes mellitus as an initial symptom.

Authors:  Koko Nemoto; Kentaro Sano; Satoko Sato; Yasuhiro Maeda; Kei Murayama; Jun-Ichi Takanashi
Journal:  Radiol Case Rep       Date:  2022-06-17

4.  Genetic and Mitochondrial Metabolic Analyses of an Atypical Form of Leigh Syndrome.

Authors:  Martine Uittenbogaard; Kuntal Sen; Matthew Whitehead; Christine A Brantner; Yue Wang; Lee-Jun Wong; Andrea Gropman; Anne Chiaramello
Journal:  Front Cell Dev Biol       Date:  2021-12-22

5.  Leukocytes mediate disease pathogenesis in the Ndufs4(KO) mouse model of Leigh syndrome.

Authors:  Julia C Stokes; Rebecca L Bornstein; Katerina James; Kyung Yeon Park; Kira A Spencer; Katie Vo; John C Snell; Brittany M Johnson; Philip G Morgan; Margaret M Sedensky; Nathan A Baertsch; Simon C Johnson
Journal:  JCI Insight       Date:  2022-03-08
  5 in total

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