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- Disease Information
- Disease Comparison
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Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
- Congenital-developmental
- Deficiency
- Degenrative-Necrosis
- Electromagnetic-Physics
- Eponymic
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- Idiopathic
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Major Organs-Systems ▼
- Systemic
- Pediatric
- Nervous & Sensory System (Neurology)
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- Respiratory (Pulmonary) System
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- Urinary System
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- Musculoskeletal System
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- Tissue/Cells/Organelles
Disease Information for Antithrombin III deficiency, familial
- Clinical Manifestations
- Signs & Symptoms
- Signs of phlebitis in leg
- Moro Reflex unilateral Abnormal
- Stroke Syndrome Child
- Stroke syndrome/signs
- Clinical Presentation & Variations
- Presentation/Deep Vein Thrombosis Young Recurrent
- Presentation/Thrombophlebitis Hereditary Recurrent
- Presentation/Pulmonary Embolism Recurrent
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Demographics & Risk Factors
- Population Group
- Child
- Population/Pediatrics population
- Family History
- Family history/Thrombosis/DVT/Deaths
- Sex & Age Groups
- Population/Child
- Population/Children/all
- Laboratory Tests
- Abnormal Lab Findings - Decreased
- Antithrombin III (Lab)
- Abnormal Lab Findings - Increased
- Fibrin Degredation Product (FDP) (Lab)
- Fibrin Split Products/FSP/Dimers/Monomers (Lab)
- FibrinPeptide A
- Soluble Fibrin Monomers [LAB]
- Associated Diseases & Rule outs
- Rule Outs
- Antiphospholipid Syndrome/APLS
- Associated Disease & Complications
- Cerebral vascular accident
- Cerebral vein thrombosis/phlebitis
- Heparin resistance syndrome
- Hypercoagulability/Thrombophilia
- Mesenteric vein thrombosis
- Migratory superficial phlebitis
- Pulmonary embolism
- Purpura fulminans
- Retinal vein thrombosis, central
- Splenic infarction
- Stroke Syndromes/Atypical causes
- Stroke/Child
- Thromboembolic disease
- Thrombophlebitis Arm/Deep Vein
- Thrombophlebitis, deep vein
- Transient ischemic attack/cerebral
- Warfarin induced/skin necrosis
- Hypercoaguability
- Disease Mechanism & Classification
- Class
- CLASS/Hematologic (category)
- Pathophysiology
- Pathophysiology/Gene locus 1q23-q25
- Pathophysiology/Gene locus Chromosome 1
- Pathophysiology/Gene Locus Identified/OMIM database
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Hereditary disease/Adult manifestations
- Pathophysiology/Antithrombin III defect/deficiency
- Pathophysiology/Intravasular coagulation process
- Pathophysiology/Spontaneous Coagulation
- Pathophysiology/Ischemic optic neuritis
- Process
- PROCESS/Enzyme defect/Metabolic disorder (ex)
- PROCESS/Hereditofamilial (category)
- PROCESS/Metabolic/storage disorder (category)
- PROCESS/Coagulation derangement/disorder (ex)
- PROCESS/Hereditary hypercoagulation/thrombosis disorders (ex)
- Synonyms
- Synonym
- Antithombin III deficiency, ANTITHROMBIN 3 DEFIC, Antithrombin 3 Deficiencies, Antithrombin 3 Deficiency, Antithrombin deficiency, ANTITHROMBIN III DEFIC, Antithrombin III Deficiencies, Antithrombin III deficiency, Antithrombin III deficiency (disorder), AT def Antithrombin defi, AT deficiency Antithrombin deficiency, DEFIC ANTITHROMBIN III, Deficiencies Antithrombin 3, Deficiencies Antithrombin III, Deficiency Antithrombin 3, Deficiency Antithrombin III, Familial, Synonym/Antithrombin deficiency, Synonym/Factor XIV deficiency
- Treatment
- Drug Therapy - Contraindication
- RX/Oral contraceptive
- Drug Therapy - Indication
- RX/Anticoagulants
- RX/Coumarin/derivatives
- RX/Warfarin (Coumadin)
- Other Treatments
- TX/Lifetime anticoagulation
- Definition
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Antithrombin III Deficiency: Synonyms for this familial thromboembolic, thrombophlenitis syndrome include; AT 3,AT III Deficiency; Thrombophilia, Hereditary Due to AT III; Note Disorder Subdivisions: AT III Variant IA; AT III Variant Ib;Antithrombin III Deficiency, Classical (Type I).
Discussion: Antithrombin III (AT III) deficiency is a blood disorder characterized by the tendency to form clots in the arteries and/or veins (thrombosis); An inherited tendency to thrombosis is known as thrombophilia; Antithrombin III is a substance in the blood that limits the blood"s ability to clot (coagulation); In people with congenital antithrombin III deficiency, there is usually a reduced amount of this substance in the blood due to a genetic abnormality; Antithrombin III deficiency may also be acquired; in such cases, the disorder may be reversible with treatment--------------[NORD 2005]--------------
(Edit)
- External Links Related to Antithrombin III deficiency, familial
- Wikipedia
- Merck
- Images
- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)
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