Hyperprothrombinemia

Hyperprothrombinemia is a medical condition characterized by an abnormally high level of prothrombin, a protein in the blood that aids in blood clotting. This condition can lead to an increased risk of thrombosis, or blood clots.

Causes

Hyperprothrombinemia can be caused by a variety of factors, including genetic mutations, certain medications, and liver disease. The most common genetic mutation associated with this condition is the G20210A mutation in the prothrombin gene.

Symptoms

The primary symptom of hyperprothrombinemia is an increased risk of developing blood clots. These clots can lead to serious health complications, such as deep vein thrombosis, pulmonary embolism, and stroke. Other symptoms can include bruising, bleeding, and pain in the affected area.

Diagnosis

Hyperprothrombinemia is typically diagnosed through a blood test that measures the level of prothrombin in the blood. Genetic testing may also be performed to identify any mutations in the prothrombin gene.

Treatment

Treatment for hyperprothrombinemia typically involves managing the risk of blood clots. This can include the use of anticoagulant medications, lifestyle changes, and in some cases, surgical procedures.

See also

• Prothrombin time
• Coagulation
• Thrombophilia

References

Hyperprothrombinemia Resources
Need Help Finding a Doctor? Need help finding a doctor or specialist anywhere in the world? Explore our world directory. WikiMD's DocFinder can assist you in locating millions of physicians.	Medical Knowledge Access the latest research - Most recent articles Ongoing trials.

Translate to: East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski