Antithrombin III Deficiency |
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Antithrombin III deficiency is a genetic disorder that causes the blood to clot abnormally.
Causes, incidence, and risk factors: ...
Congenital antithrombin III deficiency is a genetic disorder that causes the blood to clot more than normal.
Alternative Names
Deficiency - antithrombin III - congenital; Antithrombin III deficiency - congenital ...
Antithrombin III deficiency
Antithrombin III deficiency is a rare haematological hereditary disorder which is often diagnosed when the patient experiences recurrent venous thrombosis (blood clot found in the veins) and pulmonary embolism (when a ...
Antithrombin III Deficiency, Classical (Type I)
AT III Variant IA
AT III Variant Ib
General Discussion ...
Antithrombin III deficiency
Factor V Leiden mutation (activated protein C resistance)
Heparin Some Trade Names
HEPFLUSH-10
Click for Drug Monograph
-induced thrombocytopenia and thrombosis ...
primary: Antithrombin III deficiency Â- Protein C deficiency/Activated protein C resistance/Protein S deficiency/Factor V Leiden Â- Hyperprothrombinemia ...
Deficiency - antithrombin III - congenital (Congenital antithrombin III deficiency)
Deficiency - B12 (Vitamin B12)
Deficiency - folic acid, Folic acid deficiency (Folate deficiency)
Deficiency - niacin (Pellagra)
Deficiency - vitamin B1 (Thiamine) ...
Congenital antithrombin III deficiency
Congenital protein C or S deficiency
Disseminated intravascular coagulation (DIC)
Drug-induced immune thrombocytopenia
Factor II deficiency
Factor V deficiency
Factor VII deficiency
Factor X deficiency ...
Does individual have glomerulopathic disease, systemic lupus erythematosus, renal cell carcinoma, antithrombin III deficiency, or substance P deficiency?
Antithrombin III is a protein in the blood that blocks blood clots from forming. Congenital antithrombin III deficiency is a genetic disease. It occurs when a person receives one abnormal copy of a gene from a parent with the disease.
Hypercoagulable states (diseases that increase blood clotting), such as protein C and S deficiency and antithrombin III deficiency
Cancer
Examination: ...
Common mutations include Factor V Leiden and Prothrombin G20210A mutations. Fairly rare genetic mutations include proteins C and S deficiencies and antithrombin III deficiency.
Medicines ...
Pulmonary ventilation/perfusion scan
Phenytoin overdose
Total anomalous pulmonary venous return
Calcium - ionized
Diphtheria immunization (vaccine)
Congenital antithrombin III deficiency
Partial complex seizure ...
Congenital antithrombin III deficiency
Congenital bronchiectasis
Congenital cataract
Congenital CMV
Congenital cranial osteoporosis
Congenital cytomegalovirus
Congenital dermal melanocytosis
Congenital dislocation of the hip ...
Antithrombin III deficiency, congenital ... pulmonary embolism
Antley-Bixler Syndrome ... depressed nasal bridge
Antley-Bixler-like syndrome -- ambiguous genitalia -- disordered steroidogenesis ... depressed nasal bridge
Antlophobia ...
 See also: Antithrombin III, Deficiency, Congenital antithrombin III deficiency, Symptom, Thrombosis
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