| Literature DB >> 34802542 |
James A Poulter1, Sinisa Savic2.
Abstract
Systemic autoinflammatory disorders (SAIDs) encompass a heterogeneous group of monogenic disorders characterized by recurrent episodes of systemic and organ-specific inflammation. Genetic studies have facilitated the identification of Mendelian forms of SAIDs but many patients still remain without a diagnosis. Recent studies have uncovered that somatic (acquired) mutations can cause later-onset SAIDs. In this review, we will discuss the current knowledge surrounding the genetics of these acquired auto-inflammatory disorders (AAIDs), with a focus on VEXAS, NLRP3-associated AAIDs and Schnitzler's syndrome and provide suggestions for future research in this field.Entities:
Keywords: Auto-Inflammatory Disease; NLRP3; SAID; Schnitzler's syndrome; UBA1; VEXAS
Mesh:
Year: 2021 PMID: 34802542 DOI: 10.1053/j.seminhematol.2021.10.001
Source DB: PubMed Journal: Semin Hematol ISSN: 0037-1963 Impact factor: 3.851