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Hereditary systemic autoinflammatory diseases and Schnitzler's syndrome [Elektronski vir]Kačar, Mark ; Pathak, Shelly ; Savic, SinisaThe systemic autoinflammatory diseases are disorders of the innate immune system distinguished by severe inflammation resulting from dysregulation of the innate immune system. Hereditary fever ... syndromes, such as FMF, TNF receptor-associated periodic syndrome, cryopyrin-associated periodic syndromes and mevalonate kinase deficiency, were the first group of systemic autoinflammatory diseases for which a genetic basis was established, between 1999 and 2001. Currently according to the latest report of the international union of immunological societies, 37 separate monogenic disorders were classified as autoinflammatory. In addition to the abovementioned monogenic conditions, we describe Schnitzler's syndrome, a well-defined, acquired autoinflammatory condition without a clear genetic basis. For the purposes of this review, we discuss several conditions defined by the latest consensus process as systemic autoinflammatory diseases. We focus on those disorders where recent studies have contributed to further phenotypic characterization or had an impact on clinical management.Vir: Rheumatology. - ISSN 1462-0332 (Vol. 58, suppl. 6, Nov. 2019, str. vi31-vi43)Vrsta gradiva - e-članek ; neleposlovje za odrasleLeto - 2019Jezik - angleškiCOBISS.SI-ID - 58561539
Avtor
Kačar, Mark |
Pathak, Shelly |
Savic, Sinisa
Teme
Pyrin |
Schnitzler syndrome |
Haploinsufficiency |
Pirin |
Schnitzlerjev sindrom |
Haploinsuficienca |
autoinflammatory diseases |
pyrin-associated autoinflammatory diseases |
NLRP3-related autoinflammatory diseases |
undifferentiated systemic autoinflammatory disease |
relopathies |
avtovnetne bolezni |
s pirinom povezane avtovnetne bolezni |
z NLRP3 povezane avtovnetne bolezni |
relopatije
Vnos na polico
Trajna povezava
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