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临床免疫学综述系列:周期性发热综合征患者的处理方法。

Clinical immunology review series: An approach to the patient with a periodic fever syndrome.

机构信息

National Amyloidosis Centre and Centre for Amyloidosis and Acute Phase Proteins, Division of Medicine, University College London Medical School, Royal Free Campus, London, UK.

出版信息

Clin Exp Immunol. 2011 Sep;165(3):301-9. doi: 10.1111/j.1365-2249.2011.04438.x. Epub 2011 Jul 7.

Abstract

The periodic fever syndromes are disorders of innate immunity. They may be inherited or acquired and present as recurrent attacks of apparently spontaneous self-limiting inflammation without evidence of autoantibodies or infection. Over the past decade-and-a-half there has been significant progress in their understanding and treatment.

摘要

周期性发热综合征是先天性免疫紊乱。它们可能是遗传性的或获得性的,表现为反复发作的、明显自发的、自限性炎症,无自身抗体或感染的证据。在过去的十几年中,人们对它们的认识和治疗取得了显著进展。

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本文引用的文献

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The Schnitzler syndrome. Schnitzler 综合征。
Orphanet J Rare Dis. 2010 Dec 8;5:38. doi: 10.1186/1750-1172-5-38.
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Differentiating PFAPA syndrome from monogenic periodic fevers.区分PFAPA综合征与单基因周期性发热。
Pediatrics. 2009 Oct;124(4):e721-8. doi: 10.1542/peds.2009-0088. Epub 2009 Sep 28.
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Dysfunctional inflammasome in Schnitzler's syndrome.
Rheumatology (Oxford). 2009 Oct;48(10):1304-8. doi: 10.1093/rheumatology/kep222. Epub 2009 Aug 20.
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The clinical spectrum of 94 patients carrying a single mutated MEFV allele.94例携带单个MEFV等位基因突变患者的临床谱。
Rheumatology (Oxford). 2009 Jul;48(7):840-2. doi: 10.1093/rheumatology/kep121. Epub 2009 May 22.

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