Clinical Phenotypes of Adult-Onset Still’s Disease: New Insights from Pathophysiology and Literature Findings

Adult-onset Still’s disease (AOSD) is a non-familial, polygenic systemic autoinflammatory disorder. It is traditionally characterized by four cardinal manifestations—spiking fever, an evanescent salmon-pink maculopapular rash, arthralgia or arthritis and a white-blood-cell count (WBC) ≥ 10,000/mm(3)...

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Detalles Bibliográficos
Autores principales: Mitrovic, Stéphane, Fautrel, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232697/
https://www.ncbi.nlm.nih.gov/pubmed/34203779
http://dx.doi.org/10.3390/jcm10122633

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232697/
https://www.ncbi.nlm.nih.gov/pubmed/34203779
http://dx.doi.org/10.3390/jcm10122633

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