Title of article
Overt and occult rheumatic diseases: the child with chronic fever
Author/Authors
Joost Frenkel، نويسنده , , Wietse Kuis، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2002
Pages
27
From page
443
To page
469
Abstract
Identification of the genes involved in hereditary periodic fever syndromes has led to the recognition of a new pathophysiological category, the autoinflammatory disorders. The main non-hereditary autoinflammatory disease in childhood is systemic juvenile idiopathic arthritis (sJIA), others being the chronic infantile neurological cutaneous arthropathy (CINCA) syndrome and the periodic fever, aphthous stomatitis, pharyngitis and adenopathy (PFAPA) syndrome. Familial Mediterranean fever (FMF) has been traced to mutations in the MEFV gene. Mutations in the MVK gene, encoding the enzyme mevalonate kinase, cause the hyper-IgD periodic fever syndrome (HIDS). The tumour necrosis factor(TNF)-receptor-associated periodic syndromes (TRAPS) have been linked to mutations in theTNFRSF1Agene, encoding a TNF-α receptor, and the CIAS1 gene is mutated in familial cold autoinflammatory syndrome. We discuss how this knowledge has influenced diagnosis and treatment of these rare genetic disorders and how it might change our approach to the more common rheumatic diseases.
Keywords
genetics , child , inflammation , Treatment , human , diagnosis , tumour necrosis factor , arthritis , IgA , mutation , traps , Fever , Familial Mediterranean fever , Hereditary , fever of unknown origin , autoinflammatory , immunoglobulin D , IgD , Hibernian fever , Muckle–Wells syndrome , systemic juvenile idiopathic arthritis
Journal title
Best Practice and Research Clinical Rheumatology
Serial Year
2002
Journal title
Best Practice and Research Clinical Rheumatology
Record number
466960
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