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dc.contributor.authorAbdullaeva Umida Kurbanovna, Nabieva Dildora Abdumalikovna, Yusupov Ilkhom Kobulzhonovich-
dc.date.accessioned2024-01-15T01:37:22Z-
dc.date.available2024-01-15T01:37:22Z-
dc.date.issued2023-08-
dc.identifier.issn2181-712Х-
dc.identifier.urihttp://repository.tma.uz/xmlui/handle/1/10060-
dc.description.abstractSystemic sclerosis, or systemic scleroderma (SSD), is an autoimmune disease of connective tissue, the main clinical signs of which are caused by widespread microcirculation disorders, fibrosis of the skin and internal organs. According to morphological studies, 80% of patients with SSD have kidney changes, including those not associated with rheumatic diseases. While the prevalence of sclerodermic renal crisis is currently estimated at 2-5%, an asymptomatic decrease in renal function ("mute uremia") due to the presence of multimorbid and comorbid pathology is much more often noted. Its frequency in patients with SSD can reach 55%.en_US
dc.language.isootheren_US
dc.publisherТиббиётда янги кунen_US
dc.subjectsystemic scleroderma; sclerodermic renal crisis; vascular endothelial dysfunction; chronic sclerodermic nephropathy; nonimmune factors of nephropathy progression; chronic kidney disease.en_US
dc.titleModern concepts of kidney damage in patients with systemic sclerodermaen_US
dc.typeArticleen_US
Appears in Collections:Thesis, Articles

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