Prothrombin Mutation

Prothrombin mutation is a genetic change that affects a gene responsible for producing a protein called prothrombin, which plays a key role in blood clotting. This mutation can increase the risk of forming abnormal blood clots, especially in veins, leading to conditions such as deep vein thrombosis or pulmonary embolism. People with this mutation may not show symptoms but are at higher risk if they experience situations that promote clotting, like surgery or prolonged immobility. It is usually inherited and can be identified through blood tests, helping manage and reduce potential complications.