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Letter to the Editor in response to Dr. Josef Finsterer et al. "Intense work-up is required for pediatric COVID-related acute necrotizing encephalopathy with RANBP2 variants".

作者信息

Suppiej Agnese, Forest Cristina

机构信息

Department of Medical Sciences-Pediatric Section, University of Ferrara, Ferrara, Italy.

Department of Medical Sciences-Pediatric Section, University of Ferrara, Ferrara, Italy.

出版信息

Eur J Paediatr Neurol. 2023 Mar;43:62. doi: 10.1016/j.ejpn.2023.02.001. Epub 2023 Feb 27.

DOI:10.1016/j.ejpn.2023.02.001
PMID:36990949
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9969750/
Abstract
摘要

相似文献

1
Letter to the Editor in response to Dr. Josef Finsterer et al. "Intense work-up is required for pediatric COVID-related acute necrotizing encephalopathy with RANBP2 variants".致编辑的信：回应约瑟夫·芬斯特勒博士等人的《伴有RANBP2变异的儿童新冠相关急性坏死性脑病需要强化检查》
Eur J Paediatr Neurol. 2023 Mar;43:62. doi: 10.1016/j.ejpn.2023.02.001. Epub 2023 Feb 27.
2
Intense work-up is required for pediatric COVID-related acute necrotizing encephalopathy with RANBP2 variants.对于患有RANBP2基因变异的小儿新冠相关急性坏死性脑病，需要进行全面细致的检查。
Eur J Paediatr Neurol. 2023 Mar;43:16-17. doi: 10.1016/j.ejpn.2023.02.002. Epub 2023 Feb 18.
3
A Rare Case of COVID-19 Related Acute Necrotizing Encephalopathy With the RANBP2 Mutation in a Pediatric Patient.儿童 COVID-19 相关急性坏死性脑病伴 RANBP2 突变的罕见病例。
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COVID-19 related acute necrotizing encephalopathy with extremely high interleukin-6 and RANBP2 mutation in a patient with recently immunized inactivated virus vaccine and no pulmonary involvement.COVID-19 相关急性坏死性脑病伴极高白细胞介素-6 和 RANBP2 突变，患者近期接种过灭活病毒疫苗且无肺部受累。
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Genetic Acute Necrotizing Encephalopathy Associated with RANBP2: Clinical and Therapeutic Implications in Pediatrics.与RANBP2相关的遗传性急性坏死性脑病：儿科临床及治疗意义
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First case with RANBP2 biallelic mutation and severe acute necrotizing encephalopathy phenotype.首例 RANBP2 双等位基因突变伴严重急性坏死性脑病表型。
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Roles of Nucleoporin RanBP2/Nup358 in Acute Necrotizing Encephalopathy Type 1 (ANE1) and Viral Infection.核孔蛋白 RanBP2/Nup358 在急性坏死性脑病 1 型 (ANE1) 和病毒感染中的作用。
Int J Mol Sci. 2022 Mar 24;23(7):3548. doi: 10.3390/ijms23073548.
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Workshop on RanBP2/Nup358 and acute necrotizing encephalopathy.RanBP2/Nup358 工作坊与急性坏死性脑病
Nucleus. 2022 Dec;13(1):154-169. doi: 10.1080/19491034.2022.2069071.

本文引用的文献

1
Recurrent acute hemorrhagic necrotizing encephalopathy associated with RAN-binding protein-2 gene mutation in a pediatric patient.一名儿科患者中与RAN结合蛋白2基因突变相关的复发性急性出血性坏死性脑病。
BJR Case Rep. 2022 Nov 1;8(6):20220019. doi: 10.1259/bjrcr.20220019.
2
Pediatric recurrent acute necrotizing encephalomyelitis, RANBP2 genotype and Sars-CoV-2 infection: Diagnosis, pathogenesis and targeted treatments from a case study.儿童复发性急性坏死性脑脊髓炎、RANBP2 基因型与 SARS-CoV-2 感染：来自病例研究的诊断、发病机制与靶向治疗。
Eur J Paediatr Neurol. 2023 Jan;42:117-121. doi: 10.1016/j.ejpn.2022.12.010. Epub 2023 Jan 4.
3
Roles of Nucleoporin RanBP2/Nup358 in Acute Necrotizing Encephalopathy Type 1 (ANE1) and Viral Infection.核孔蛋白 RanBP2/Nup358 在急性坏死性脑病 1 型 (ANE1) 和病毒感染中的作用。
Int J Mol Sci. 2022 Mar 24;23(7):3548. doi: 10.3390/ijms23073548.