# Unlucky for some? Bleeding associated with factor XIII deficiency during extracorporeal membrane oxygenation

**Authors:** Andrew J. Doyle

PMC · DOI: 10.1016/j.rpth.2026.103363 · Research and Practice in Thrombosis and Haemostasis · 2026-02-06

## Full-text entities

- **Genes:** F13A1 (coagulation factor XIII A chain) [NCBI Gene 2162] {aka F13A}, VWF (von Willebrand factor) [NCBI Gene 7450] {aka F8VWF, VWD}, PLG (plasminogen) [NCBI Gene 5340] {aka HAE4}, F8 (coagulation factor VIII) [NCBI Gene 2157] {aka AHF, DXS1253E, F8B, F8C, FVIII, HEMA}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}
- **Diseases:** factor XIII deficiency (MESH:D005177), hypofibrinogenemia (MESH:D000347), von Willebrand dysfunction (MESH:D014842), autoimmunity (MESH:D001327), Bleeding (MESH:D006470), COVID-19 infection (MESH:D000086382), thrombocytopenia (MESH:D013921), malignancy (MESH:D009369), coagulation defects (MESH:D001778), FXIII deficiency (MESH:D007153), death (MESH:D003643), platelet dysfunction (MESH:D001791), thrombotic (MESH:D013927), critical illness (MESH:D016638), trauma (MESH:D014947)
- **Chemicals:** ammonia (MESH:D000641)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC12930158/full.md

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Source: https://tomesphere.com/paper/PMC12930158