Literature DB >> 29860887

[Autoinflammatory diseases].

Bernadett Mosdósi1, Beáta Tóth2.   

Abstract

Autoinflammatory diseases are disorders of the innate immune system characterized by recurrent systematic inflammation and serious complications. Dysregulation of inflammasome and overproduction of interleukin-1 play a major role in the pathogenesis of autoinflammatory diseases. The diagnosis of these rare conditions rely on recognising the pattern of presentation and differential diagnosis. Manifestations may include fever, rash, serositis (pleuritis and peritonitis), arthritis, meningitis and uveitis. Secondary amyloidosis may complicate longstanding disease. Advances in our understanding of the molecular and pathophysiological basis of the autoinflammatory diseases have resulted in new treatment strategies. Early diagnosis and effective therapy are critical to prevent irreversible organ damage. The purpose of this review is to describe the major clinical, genetic, and therapeutic features of the most common autoinflammatory syndromes. Orv Hetil. 2018; 159(23): 898-907.

Entities:  

Keywords:  autoinflammatiós kórképek; autoinflammatory disorders; fever; inflammasoma; inflammasome; interleukin-1; láz

Mesh:

Year:  2018        PMID: 29860887     DOI: 10.1556/650.2018.31068

Source DB:  PubMed          Journal:  Orv Hetil        ISSN: 0030-6002            Impact factor:   0.540


  1 in total

1.  Mevalonate kinase deficiency/Hyperimmunoglobulin D syndrome (MVK/HIDS) in a Differential Diagnosis of Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Cervical Adenitis (PFAPA) Syndrome and Familial Mediterranean Fever (FMF): A Case Report.

Authors:  Berkay Aktaş; Diyar Gümüş; Atacan Tunalı; Ziya Kunter; Amra Adrovic
Journal:  Turk Arch Pediatr       Date:  2022-05
  1 in total

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