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Prothrombin Gene Mutation

Prothrombin gene mutation is a genetic change that affects the prothrombin protein, which is crucial for blood clotting. This mutation can lead to higher levels of prothrombin in the blood, increasing the risk of abnormal blood clots (thrombosis). These clots can form in veins, such as in deep vein thrombosis or pulmonary embolism, and can cause serious health issues. It's an inherited condition, meaning it can run in families. Individuals with this mutation may require monitoring and preventive measures to manage their risk of developing clots.

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    Prothrombin gene mutation is a hereditary condition that affects the blood's ability to clot. It involves a change in the prothrombin gene, which provides instructions for making prothrombin, a protein essential for blood clotting. This mutation can lead to higher levels of prothrombin in the blood, increasing the risk of abnormal blood clots, known as thrombosis. Such clots can occur in veins or arteries and may lead to serious health issues, including deep vein thrombosis or pulmonary embolism. Regular monitoring and management can help individuals with this mutation reduce their risk of complications.