Stuart Prower deficiency, also known as protein C deficiency, refers to a rare genetic disorder that affects the blood's ability to clot properly. This condition is caused by a deficiency in the protein C, which plays a crucial role in regulating blood clotting. Patients with Stuart Prower deficiency may experience an increased risk of blood clot formation, leading to potentially dangerous complications such as deep vein thrombosis or pulmonary embolism. Synonyms for Stuart Prower deficiency include protein C deficiency, protein C deficiency disease, and genetic clotting disorder. Early diagnosis and appropriate medical management are essential to minimize the risk of clot-related complications and ensure a healthy life for individuals with this condition.