Trastornos autoinflamatorios: un nuevo concepto en s赤ndromes de fiebre recurrente hereditaria

作者：Horcada Rubio; M L; Delgado Beltran; C; Armas Ramirez; C

来源：Anales de Medicina Interna, 2004.

DOI：10.4321/S0212-71992004000300011

• autoinflammatory sindromes
• periodic fever familial mediterranean fever (fmf)
• hiper ig-d syndrome (hids)
• tnf-receptor-associated periodic syndrome (traps)
• muckle-wells syndrome (mws)
• familial cold autoinflammatory syndrome (fcas)
• cinca syndrom.

at last year the great scientific advances in genetics and molecular biology have led to a bigger knowledge about we nowadays call ※ autoinflammatory syndromes§, characterized by recurrent inflammatory episodes genetically determined and not mediated by autoinmmunity. in this group, they are included the hereditary periodic fever syndromes: familial mediterranean fever (fmf), hiper ig-d syndrome (hids), tnf-receptor-associated periodic syndrome (traps), muckle-wells syndrome (mws), familial cold autoinflammatory syndrome (fcas), cinca syndrome. the past 6 year have witnessed the identification of genes causing these diseases. some of these genes encode proteins with a common domain ( pyrin domain). these protein are part of regulatory pathway of inflammationand apoptosis. the purpose of this article, is to carry out review of the genetic, clinical, molecular and rheumatologic aspect of these syndromes, in part unknow. although they are not common, they are not absent in our diary clinical practise. their study and research we will be able to obtain new knowledge that lead us to solve the complex inflammatory process.