Congenital hypofibrinogenemia with bone cyst: a case report with review of literature

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Congenital hypofibrinogenemia with bleeding risk: mutations in the <i>FGA, FGB</i> , and <i>FGG</i> genes2025
2. 2Paradoxical Deep Vein Thrombosis in Congenital Hypofibrinogenemia in a Patient with Prior Severe Bleeding and Spontaneous Intracerebral Hemorrhage: A Case Report2026
3. 3Recurrent Venous Thrombosis in a Hypofibrinogenemic Patient Despite a Heterozygous Deletion of the Fibrinogen Gene Cluster and Hemizygous FGB p.Pro265Leu Variant Mimicking a Homozygous Genotype.2025
4. 4Healed retinal vasculitis in a child with hypofibrinogenemia2024
5. 5A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family2024 · 2 citations