Product was successfully added to your shopping cart.
What is Thrombophilia?
Description of the disease
Thrombophilia is an inherited or acquired condition in which the blood has an increased tendency to form blood clots. Thrombi can form in veins or arteries, which can lead to serious complications such as stroke or venous thrombosis.
Classification
Hereditary thrombophilia
Acquired thrombophilia
Symptoms
Symptoms of thrombophilia may include pain and swelling in the area of the thrombosis, shortness of breath, rapid fatigue, dizziness, as well as symptoms related to thrombosis complications.
Causes
Hereditary thrombophilia is usually associated with certain genetic mutations, while acquired thrombophilia can be caused by factors such as prolonged immobilization, pregnancy, certain diseases, and the use of certain medications.
Diagnosis
Diagnosis of thrombophilia includes performing special blood tests, including measuring the level of coagulation factors and searching for genetic mutations.
Treatment
Treatment of thrombophilia may include taking anticoagulants, as well as correcting the risk of thrombosis by changing lifestyle and applying preventive measures.
Prevention
Preventive measures include minimizing risk factors for thrombosis, regular physical exercises, weight control, and smoking cessation.
Physician
Treatment of thrombophilia is carried out by a hematologist or a therapist specializing in the field of blood and blood coagulation system.
Note: This material is provided for informational purposes only and is not medical advice.