Identification of a variant in NLRP3 gene in a patient with Muckle-Wells syndrome: a case report and review of literature

Identification of a variant in NLRP3 gene in a patient with Muckle-Wells syndrome: a case report and review of literature

Abstract Background Cryopyrin-associated periodic syndrome (CAPS), a rare genetic autoimmune disease, is composed of familial cold autoinflammatory syndrome (FCAs), Muckle-Wells syndrome (MWS), and neonatal onset multisystem inflammatory disease (NOMID). MWS is caused by dominantly inherited or de n...

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Bibliographic Details
Main Authors: Jia Liu, Ranran Zhang, Zhi Yi, Yi Lin, Hong Chang, Qiuye Zhang
Format: Article
Language:English
Published: BMC 2023-02-01
Series:Pediatric Rheumatology Online Journal
Subjects:
Cryopyrin-associated periodic syndrome (CAPS)
Muckle-Wells syndrome (MWS)
NLRP3 gene
Variation
Online Access:https://doi.org/10.1186/s12969-023-00795-x

Internet

https://doi.org/10.1186/s12969-023-00795-x

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