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Article

Novel heterozygous F7 gene mutation (c. C1286T) associated with congenital factor VII deficiency: A case report and literature review.

Journal of clinical laboratory analysis - 1 May 2022

Tang Hua, Luan Xingzhao, Li Jiaqi, Jiang Gen, Zhen Haowen, Li Hao, Xiang Wei, Zhou Jie

Abstract excerpt

BACKGROUND: Congenital factor VII (FVII) deficiency is a rare inherited autosomal recessive disorder characterized by prolongation of prothrombin time and low FVII coagulation activity, which may increase the risk of bleeding. CASE PRESENTATION: A 66-year-old man with acute postoperative intracranial hemorrhage was transferred to our hospital owing to coagulation dysfunction. In coagulation tests, the FVII...

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PMID: 35349734
DOI: 10.1002/jcla.24349
PMCID: PMC9102670

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