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Congenital antithrombin III deficiency

Disease Congenital amputationCongenital cataract

Congenital antithrombin III deficiency : Definition
Congenital antithrombin III deficiency : Overview, Causes, & Risk Factors
Congenital antithrombin III deficiency : Symptoms & Signs ...

 


Congenital antithrombin III deficiency
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Congenital Antithrombin Iii Deficiency
Congenital antithrombin III deficiency
Table of Contents ...

Definition of Congenital antithrombin III deficiency:
Antithrombin III deficiency is a genetic disorder that causes the blood to clot abnormally.
Causes, incidence, and risk factors: ...

Antithrombin III Deficiency
Congenital Antithrombin III Deficiency
See How are genetic conditions and genes named? in the Handbook.
What if I still have specific questions about hereditary antithrombin 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.

Pulmonary ventilation/perfusion scan
Phenytoin overdose
Total anomalous pulmonary venous return
Calcium - ionized
Diphtheria immunization (vaccine)
Congenital antithrombin III deficiency
Partial complex seizure ...

See also: Antithrombin III Deficiency, Antithrombin III, Deficiency, Leukemia, Symptom

Disease Congenital amputationCongenital cataract

 
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