Congenital antithrombin III deficiency
Deficiency - antithrombin III - congenital; Antithrombin III deficiency - congenital
Congenital antithrombin III deficiency is a
Deep venous thrombosis (DVT) affects mainly the veins in the lower leg and the thigh. It involves the formation of a clot (thrombus) in the larger veins of the area.
Causes
Antithrombin III is a protein in the blood that blocks abnormal blood clots from forming. It helps the body keep a healthy balance between bleeding and clotting. Congenital antithrombin III deficiency is an inherited disease. It occurs when a person receives one abnormal copy of the antithrombin III gene from a parent with the disease.
The abnormal gene leads to a low level of the antithrombin III protein. This low level of antithrombin III can cause abnormal blood clots (thrombi) that can block blood flow and damage organs.
People with this condition will often have blood clots at a young age. They are also likely to have family members who have had a blood clotting problem.
Symptoms
People will usually have symptoms of a blood clot. Blood clots in the arms or legs usually cause swelling, redness, and pain. When a blood clot breaks off from where it formed and travels to another part of the body, it is called a thromboembolism. Symptoms depend on where the blood clot travels to. A common place is the lung, where the clot can cause a cough, shortness of breath, pain while taking deep breaths, chest pain, and even death. Blood clots that travel to the brain can cause a stroke.
Exams and Tests
A physical exam may show:
- A swollen leg or arm
- Decreased breath sounds in the lungs
- A rapid heart rate
The health care provider can also order a blood test to check if you have a low level of antithrombin III.
Treatment
A blood clot is treated with blood-thinning medicines (also called anticoagulants). How long you need to take these drugs depends on how serious the blood clot was and other factors. Discuss this with your provider.
Support Groups
More information and support for people with congenital antithrombin III deficiency and their families can be found at:
- National Organization for Rare Disorders --
rarediseases.org/rare-diseases/antithrombin-deficiency/ - MedlinePlus --
medlineplus.gov/genetics/condition/hereditary-antithrombin-deficiency/ - National Blood Clot Alliance --
www.stoptheclot.org/programs-services/
Outlook (Prognosis)
Most people have a good outcome if they stay on anticoagulant medicines.
Possible Complications
Blood clots can cause death. Blood clots in the lungs are very dangerous.
When to Contact a Medical Professional
See your provider if you have symptoms of this condition.
Prevention
Once a person is diagnosed with antithrombin III deficiency, all close family members should be screened for this disorder. Blood thinning drugs can prevent blood clots from forming and prevent complications from clotting.
References
Anderson JAM, Weitz JI. Hypercoagulable states. In: Hoffman R, Benz EJ, Silberstein LE, Heslop HE, Weitz JI, Salama ME, et al, eds. Hematology: Basic Principles and Practice. 8th ed. Philadelphia, PA: Elsevier; 2023:chap 138.
Mhyre JM. Hematologic and coagulation disorders. In: Chestnut DH, Wong CA, Tsen LC, et al, eds. Chestnut's Obstetric Anesthesia: Principles and Practice. 6th ed. Philadelphia, PA: Elsevier; 2020:chap 44.
Schafer AI. Thrombotic disorders: hypercoagulable states. In: Goldman L, Schafer AI, eds. Goldman-Cecil Medicine. 26th ed. Philadelphia, PA: Elsevier; 2020:chap 73.
Version Info
Last reviewed on: 2/2/2023
Reviewed by: Mark Levin, MD, Hematologist and Oncologist, Monsey, NY. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.
