PO48 | Thrombotic risk evaluation and thrombophilia testing in beta-thalassemia patients: a retrospective cohort analysis from a reference regional center

Background: β-thalassemia (βT) is a group of inherited hemoglobin synthesis disorders, characterized by defective β-chain synthesis. Clinical complications related to hemostasis, including pulmonary hypertension, venous thromboembolism (VTE), and ischemic arterial events, occur in βT with a prevale...

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Format: Article
Language:English
Published: PAGEPress Publications 2025-08-01
Series:Bleeding, Thrombosis and Vascular Biology
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Online Access:https://www.btvb.org/btvb/article/view/317
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