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Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus
Authors:Al-Mayouf Sulaiman M  Sunker Asma  Abdwani Reem  Abrawi Safiya Al  Almurshedi Fathiya  Alhashmi Nadia  Al Sonbul Abdullah  Sewairi Wafaa  Qari Aliya  Abdallah Eiman  Al-Owain Mohammed  Al Motywee Saleh  Al-Rayes Hanan  Hashem Mais  Khalak Hanif  Al-Jebali Latifa  Alkuraya Fowzan S
Institution:Rheumatology Section, Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Abstract:Systemic lupus erythematosus (SLE) is a complex autoimmune disease that causes substantial morbidity. As is typical for many other multifactorial disorders, much of the heritability of SLE remains unknown. We identified a rare autosomal recessive form of SLE, in which autozygome analysis revealed a null mutation in the DNASE1L3 gene. The DNASE1L3-related SLE we describe was always pediatric in onset and correlated with a high frequency of lupus nephritis. Our findings confirm the critical role of impaired clearance of degraded DNA in SLE pathogenesis.
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