Skip to main content
Pediatric Rheumatology logoLink to Pediatric Rheumatology
. 2015 Sep 28;13(Suppl 1):P211. doi: 10.1186/1546-0096-13-S1-P211

CIAS1-associated autoinflammatory syndrome first diagnosed at age 48 years: a case report

M Fasshauer 1,2,, S Borte 1,2, A Hauenherm 1, E Braun 1,2, H Reichenbach 3, M Borte 1,2
PMCID: PMC4599762

Cryopyrin-associated periodic syndromes are a group of autoinflammatory syndromes caused by mutations of the CIAS1gene (currently named NLRP3), and are characterized by periodic attacks of an urticaria-like rash, fever, headache, conjunctivitis and arthralgia. Often patients present in early childhood, but the great diversity of manifestations and the difficulties in genetic analyses make the diagnosis of these diseases a challenge. The authors describe the clinical features of a male patient who presented first symptoms approximately at age 23 years. with recurrent fevers up to 40°C, urticaria-like rash, orbital swelling, headache and fatigue. CIAS1-associated autoinflammatory syndrome was diagnosed at age 48 years. and confirmed genetically (mutation: c.598G>A (p.Val200Met) in Exon 3 of NLRP3 (CIAS1)-gene.

Written informated consent for publication of their clinical details was obtained from the patient/parent/guardian/relative of the patient.


Articles from Pediatric Rheumatology Online Journal are provided here courtesy of BMC

RESOURCES