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Muckle–Wells syndrome: clinical perspectives
Muckle–Wells syndrome (MWS) is a rare autoinflammatory disorder. It is due to NLRP3 gene mutations, responsible for excessive caspase-1 activation and interleukin 1β processing. MWS is the intermediate phenotype of severity of cryopyrin-associated periodic syndrome. Urticarial rash, conjunctivitis,...
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| Publicado no: | Open Access Rheumatol |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove Medical Press
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5513904/ https://ncbi.nlm.nih.gov/pubmed/28744167 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/OARRR.S114447 |
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