Severe systemic thrombosis in a young COVID-19 patient with a rare homozygous prothrombin G20210A mutation

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 investigated.PMID:34061792
Source: Infezioni in Medicina - Category: Infectious Diseases Authors: Source Type: research