Review
Open access
Sep 2026
Compound Heterozygous Mutations in FGA Cause Congenital Afibrinogenemia: A Case Report and Literature Review
Congenital afibrinogenemia is an extremely rare autosomal recessive bleeding disorder with an estimated incidence of one in one million, caused by mutations in the fibrinogen‐encoding genes.
Liang-Liang Liu, De-Sheng Yuan, Hua-Xing Zhao et al.
· Birth Defects Research · 0 citations