COVID-19 patients may experience a hypercoagulable condition, leading to thrombotic events. We describe a patient with COVID-19, carrying a rare homozygous mutation of the prothrombin gene, who developed a severe systemic vein thrombosis. In COVID-19 patients with hypercoagulability disorders the most common inherited and acquired risk factors should be investi-gated.

Severe systemic thrombosis in a young COVID-19 patient with a rare homozygous prothrombin g20210a mutation

Fiore J. R.;Margaglione M.;Santantonio T.
2021-01-01

Abstract

COVID-19 patients may experience a hypercoagulable condition, leading to thrombotic events. We describe a patient with COVID-19, carrying a rare homozygous mutation of the prothrombin gene, who developed a severe systemic vein thrombosis. In COVID-19 patients with hypercoagulability disorders the most common inherited and acquired risk factors should be investi-gated.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11369/415936
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