Conditions / Genetic
antithrombin III deficiency
info · Genetic · ICD-10: D68.59
A thrombophilia that is characterized by the tendency to form clots in the veins.
Signs and symptoms
- Decreased level of heparin co-factor II
- Recurrent thrombophlebitis
- Arterial occlusion
- Reduced antithrombin III activity
- Deep venous thrombosis
- Cerebral venous thrombosis
- Pulmonary embolism
Medications that may treat it
antithrombin III estrogens, conjugated (USP) estrone
Also known as: AT III deficiency; hereditary thrombophilia due to congenital antithrombin deficiency