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作 者:Feng Liao Jun-Ling Zeng Jian-Gang Pan Jing Ma Zhi-Jian Zhang Zhi-Jun Lin Li-Feng Lin Yu-Sen Chen Xiao-Tang Ma
机构地区:[1]Department of Neurology,Affiliated Hospital of Guangdong Medical University,Zhanjiang 524001,Guangdong Province,China [2]Guangdong Key Laboratory of Age-Related Cardiac and Cerebral Diseases,Affiliated Hospital of Guangdong Medical University,Zhanjiang 524001,Guangdong Province,China
出 处:《World Journal of Clinical Cases》2022年第2期618-624,共7页世界临床病例杂志
基 金:Supported by the Affiliated Hospital of Guangdong Medical University,No.LCYJ2018C009.
摘 要:BACKGROUND The hereditary antithrombin(AT)deficiency caused by SERPINC1 gene mutation is an autosomal dominant thrombotic disorder.An increasing number of studies have shown that mutations in the SERPINC1 rs2227589 polymorphic site are correlated with a risk of venous thromboembolism(VTE)at common sites,such as lower extremity deep venous thrombosis and pulmonary thromboembolism.Currently,there are no reports of cerebral venous sinus thrombosis(CVST),a VTE site with a low incidence rate and rs2227589 polymorphism.CASE SUMMARY Here,we report a Chinese CVST case with a mutation of the SERPINC1 rs2227589 polymorphic site,which did not cause significant AT deficiency.In a 50-year-old male patient presenting with multiple cerebral venous sinus thromboses no predisposing factors were detected,although a relative had a history of lower extremity deep venous thrombosis.We performed sequencing of the SERPINC1 gene for the patient and his daughter,which revealed the same heterozygous mutation at the rs2227589 polymorphic site:c.41+141G>A.CONCLUSION The results showed that more studies should be conducted to assess the correlation between rs2227589 polymorphism and CVST.
关 键 词:Cerebral venous sinus thromboses SERPINC1 rs2227589 polymorphic Deep venous thrombosis Venous thromboembolism Case report
分 类 号:R743[医药卫生—神经病学与精神病学]
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