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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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Detalles Bibliográficos
Autor principal:	Tran, Tu-Anh
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Dove Medical Press 2017
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513904/ https://www.ncbi.nlm.nih.gov/pubmed/28744167 http://dx.doi.org/10.2147/OARRR.S114447

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