Case report: The altered rate of monocytic cell death in a patient of Muckle-Wells syndrome with atypical clinical course

Muckle-Wells syndrome (MWS) is an autosomal dominant autoinflammatory disease recognized as the intermediate phenotype of cryopyrin-associated periodic syndrome (CAPS) caused by NLRP3 gene mutation. It often takes a long time before the diagnosis is made because the clinical presentation of MWS is v...

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Detalles Bibliográficos
Autores principales: Murakawa, Saori, Yoneda, Toru, Hoshina, Takayuki, Ishimura, Masataka, Kusuhara, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978417/
https://www.ncbi.nlm.nih.gov/pubmed/36873639
http://dx.doi.org/10.3389/fped.2023.1133097

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978417/
https://www.ncbi.nlm.nih.gov/pubmed/36873639
http://dx.doi.org/10.3389/fped.2023.1133097

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