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[Congenital Fibrinogen Deficiency Caused by Novel FGG Gene Mutation].

Zhongguo shi yan xue ye xue za zhi - 1 Apr 2021

Wang Tian-Tian, Shao Jing-Ru, Wang Jie, Cheng Yan, Zhang Xue-Qin, Fang Yun-Hai, Yao Cheng-Fang, Zhang Xin-Sheng

Abstract excerpt

OBJECTIVE: To detect and analyze coagulation related indexes and genotypes of a patient with congenital fibrinogen deficiency and his family members, and to investigate the possible molecular pathogenesis. METHODS: Four peripheral blood samples (proband and 3 family members) were collected and the prothrombin time (PT), activated partial thromboplastin time (APTT), thrombin time (TT), fibrinogen (Fg), D-Dimer and...

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PMID: 33812435
DOI: 10.19746/j.cnki.issn.1009-2137.2021.02.044

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