|
|
Congenital Antithrombin III Deficiency
Alternate Names : Antithrombin III Deficiency - Congenital, Deficiency - Antithrombin III - Congenital
Definition
Antithrombin III is a protein in the blood that blocks the formation of blood clots. Congenital antithrombin III deficiency is a genetic disease that occurs when a patient has received one abnormal copy of a gene from a parent with the disease (an autosomal dominant trait). The abnormal gene leads to low levels of antithrombin III. These low levels of antithrombin III can cause abnormal blood clots (thrombus) that may damage organs.
Pictures & Images
 See all Pictures & Images
Today's Top News Stories | • | Falls Are Top Cause of Injury, Death Among Elderly - Jul 19, 2008, 09:00
Not all homes are the same, but common sense measures can reduce the risk, expert says. | • | Heart Blood Vessels Grown in the Lab - Jul 18, 2008, 19:00
Could offer a future alternative to bypass surgery, researchers say. | • | Clinical Trials Update: July 18, 2008 - Jul 18, 2008, 09:24
- Breast Cancer
- Hot Flashes
- Emphysema
| • | Loud Music in Bars Hastens Drinking - Jul 18, 2008, 16:00
French researchers say blasting tunes makes patrons down more alcohol in less time. | • | Breast-Fed Babies Have Fewer GI Infections - Jul 18, 2008, 17:00
But they're more likely to be iron-deficient, study finds. |
|
 |
Review Date : 10/28/2003
Reviewed By : Ezra E. W. Cohen, M.D., Section of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, IL. Review provided by VeriMed Healthcare Network.
|
|
