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Rare genetic causes of meningitis and encephalitis
Differential diagnosis of meningitis and encephalitis is often very challenging because it cannot be determined based on symptoms, and the diseases have various causes. This article explains rare genetic causes of meningitis and encephalitis. Autoinflammatory disorders include cryopyrin-associated p...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Encephalitis and Neuroinflammation Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295911/ https://www.ncbi.nlm.nih.gov/pubmed/37469651 http://dx.doi.org/10.47936/encephalitis.2021.00164 |
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author | Moon, Jangsup |
author_facet | Moon, Jangsup |
author_sort | Moon, Jangsup |
collection | PubMed |
description | Differential diagnosis of meningitis and encephalitis is often very challenging because it cannot be determined based on symptoms, and the diseases have various causes. This article explains rare genetic causes of meningitis and encephalitis. Autoinflammatory disorders include cryopyrin-associated periodic syndromes, familial Mediterranean fever, and tumor necrosis factor receptor-associated periodic syndrome. Furthermore, other genetic disorders, such as complement factor I deficiency, phosphatidylinositol glycan anchor biosynthesis class T mutation, and neuronal intranuclear inclusion disease, can present as meningitis and encephalitis. |
format | Online Article Text |
id | pubmed-10295911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Korean Encephalitis and Neuroinflammation Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102959112023-07-19 Rare genetic causes of meningitis and encephalitis Moon, Jangsup Encephalitis Review Article Differential diagnosis of meningitis and encephalitis is often very challenging because it cannot be determined based on symptoms, and the diseases have various causes. This article explains rare genetic causes of meningitis and encephalitis. Autoinflammatory disorders include cryopyrin-associated periodic syndromes, familial Mediterranean fever, and tumor necrosis factor receptor-associated periodic syndrome. Furthermore, other genetic disorders, such as complement factor I deficiency, phosphatidylinositol glycan anchor biosynthesis class T mutation, and neuronal intranuclear inclusion disease, can present as meningitis and encephalitis. Korean Encephalitis and Neuroinflammation Society 2022-04 2022-02-10 /pmc/articles/PMC10295911/ /pubmed/37469651 http://dx.doi.org/10.47936/encephalitis.2021.00164 Text en Copyright © 2022 Korean Encephalitis and Neuroinflammation Society https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Moon, Jangsup Rare genetic causes of meningitis and encephalitis |
title | Rare genetic causes of meningitis and encephalitis |
title_full | Rare genetic causes of meningitis and encephalitis |
title_fullStr | Rare genetic causes of meningitis and encephalitis |
title_full_unstemmed | Rare genetic causes of meningitis and encephalitis |
title_short | Rare genetic causes of meningitis and encephalitis |
title_sort | rare genetic causes of meningitis and encephalitis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295911/ https://www.ncbi.nlm.nih.gov/pubmed/37469651 http://dx.doi.org/10.47936/encephalitis.2021.00164 |
work_keys_str_mv | AT moonjangsup raregeneticcausesofmeningitisandencephalitis |