Article

Congenital dysfibrinogenemia caused by a heterozygous mutation in the FGA gene: A case report and review of literature

2026-05-05

Abstract excerpt

<title>Abstract</title> <p>Background Congenital dysfibrinogenemia is characterized by altered functional properties of the fibrinogen; people who suffer from Congenital dysfibrinogenemia often have a low activity of fibrinogen and the mutation in the genomic DNA. Case presentation This article reports a 28-year-old pregnant woman was examined with a low congcentration of fibrinogen(Fib) and longer thrombin tim...

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Literature Corpus work: 600b8442-f540-53e0-92f2-88b0151e5c31
DOI: 10.21203/rs.3.rs-9423361/v1

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