HIGHLIGHTS
- who: Anna Sophie Wesselmann and colleagues from the USF Health, United States University of Verona, Italy have published the Article: Case report: Schnitzler-like syndrome without monoclonal gammopathy, in the Journal: (JOURNAL)
- how: To search for causative mutations in the patient the authors used a whole exome sequencing approach.
SUMMARY
Schnitzlerℓs syndrome is a rare autoinflammatory disease characterized by urticarial rash, joint pain, recurrent fever, leucocytosis, elevated C-reactive protein (CRP), and monoclonal immunoglobulin (Ig)M or IgG gammopathy. The strikingly schematic recurrence of the inflammatory episodes led the authors . . .
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