New CIAS1 mutation and anakinra efficacy in overlapping of Muckle-Wells and familial cold autoinflammatory syndromes.
case_series · Level IV
Where this comes from
- Record sourced from PubMed, PMID 18174231.
- Also identified by DOI 10.1093/rheumatology/kem318.
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Abstract
Muckle-Wells syndrome (MWS) and familial cold autoinflammatory syndrome (FCAS) are rare periodic fevers associated with CIAS1 mutations. A third entity, the chronic infantile neurological, cutaneous, articular (CINCA) syndrome was also recently associated with mutation in the same gene. A phenotypic and genotypic continuum seems to exist from the most benign (FCAS) to the most severe forms (CINCA). Although a CIAS1 mutation can be associated with two different phenotypes. We report a family of three patients exhibiting the MWS and FCAS phenotypes. These phenotypes were associated with a novel missense mutation in CIAS1. Anakinra controlled inflammatory flares in the three patients. FCAS, MWS and CINCA could be different phenotype expressions of the same disease.
Medical subject headings
- Autoimmune Diseases
- Carrier Proteins
- Genetic Predisposition to Disease
- Interleukin 1 Receptor Antagonist Protein
- Mutation, Missense