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Workshop on RanBP2/Nup358 and acute necrotizing encephalopathy

Dominant missense mutations in RanBP2/Nup358 cause Acute Necrotizing Encephalopathy (ANE), a pediatric disease where seemingly healthy individuals develop a cytokine storm that is restricted to the central nervous system in response to viral infection. Untreated, this condition leads to seizures, co...

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Autores principales: Palazzo, Alexander F., Joseph, Jomon, Lim, Ming, Thakur, Kiran T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067512/
https://www.ncbi.nlm.nih.gov/pubmed/35485383
http://dx.doi.org/10.1080/19491034.2022.2069071
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author Palazzo, Alexander F.
Joseph, Jomon
Lim, Ming
Thakur, Kiran T.
author_facet Palazzo, Alexander F.
Joseph, Jomon
Lim, Ming
Thakur, Kiran T.
author_sort Palazzo, Alexander F.
collection PubMed
description Dominant missense mutations in RanBP2/Nup358 cause Acute Necrotizing Encephalopathy (ANE), a pediatric disease where seemingly healthy individuals develop a cytokine storm that is restricted to the central nervous system in response to viral infection. Untreated, this condition leads to seizures, coma, long-term neurological damage and a high rate of mortality. The exact mechanism by which RanBP2 mutations contribute to the development of ANE remains elusive. In November 2021, a number of clinicians and basic scientists presented their work on this disease and on the interactions between RanBP2/Nup358, viral infections, the innate immune response and other cellular processes.
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spelling pubmed-90675122022-05-05 Workshop on RanBP2/Nup358 and acute necrotizing encephalopathy Palazzo, Alexander F. Joseph, Jomon Lim, Ming Thakur, Kiran T. Nucleus Meeting Report Dominant missense mutations in RanBP2/Nup358 cause Acute Necrotizing Encephalopathy (ANE), a pediatric disease where seemingly healthy individuals develop a cytokine storm that is restricted to the central nervous system in response to viral infection. Untreated, this condition leads to seizures, coma, long-term neurological damage and a high rate of mortality. The exact mechanism by which RanBP2 mutations contribute to the development of ANE remains elusive. In November 2021, a number of clinicians and basic scientists presented their work on this disease and on the interactions between RanBP2/Nup358, viral infections, the innate immune response and other cellular processes. Taylor & Francis 2022-04-29 /pmc/articles/PMC9067512/ /pubmed/35485383 http://dx.doi.org/10.1080/19491034.2022.2069071 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Meeting Report
Palazzo, Alexander F.
Joseph, Jomon
Lim, Ming
Thakur, Kiran T.
Workshop on RanBP2/Nup358 and acute necrotizing encephalopathy
title Workshop on RanBP2/Nup358 and acute necrotizing encephalopathy
title_full Workshop on RanBP2/Nup358 and acute necrotizing encephalopathy
title_fullStr Workshop on RanBP2/Nup358 and acute necrotizing encephalopathy
title_full_unstemmed Workshop on RanBP2/Nup358 and acute necrotizing encephalopathy
title_short Workshop on RanBP2/Nup358 and acute necrotizing encephalopathy
title_sort workshop on ranbp2/nup358 and acute necrotizing encephalopathy
topic Meeting Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067512/
https://www.ncbi.nlm.nih.gov/pubmed/35485383
http://dx.doi.org/10.1080/19491034.2022.2069071
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