English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Stevens-Johnson syndrome (SJS) is a complex immunological syndrome with high morbidity and mortality and characterized by acute blistering affecting the skin and at least two mucous membranes. Macrophage activation syndrome (MAS) is a severe, potentially life-threatening syndrome that often occurs in children and adults with autoimmune disease, especially systemic-onset juvenile idiopathic arthritis or adult-onset Still’s disease. This case report highlights the potential risks of SJS developing into MAS, and suggests that rapid diagnosis and treatment are essential to achieving favorable outcomes

First case report of Stevens-Johnson syndrome complicated with macrophage activation syndrome