Hereditary Antithrombin Deficiency

Common Name(s)

Hereditary Antithrombin Deficiency

Hereditary Antithrombin Deficiency is a disorder of blood clotting. People with this condition are at a higher risk of developing abnormal blood clots. Hereditary antithrombin deficiency is equally likely in men and women and runs in families. Symptoms of a blood clot due to hereditary antithrombin deficiency include coughing up blood, fainting, shortness of breath, and swelling of one leg. A physician can diagnose hereditary antithrombin deficiency with a physical exam and blood tests. The main treatment for management of hereditary antithrombin deficiency is life-long use of blood thinners.

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Advocacy and Support Organizations

 

Condition Specific Organizations

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How do you compare to others with this condition?

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Hereditary Antithrombin Deficiency" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Hereditary Antithrombin Deficiency" returned 10 free, full-text research articles on human participants. First 3 results:

Hereditary antithrombin III deficiency and neuraxial anaesthesia.
 

Author(s): B J Piper, P T Farrell

Journal: Anaesth Intensive Care. 2015 Nov;43(6):782-5.

 

Antithrombin III (ATIII) deficiency offers unique challenges to the anaesthetist in the perioperative setting due to the inherent thrombophilia, the anticoagulant therapies instituted and replacement of the deficient intrinsic natural anticoagulant. A particular challenge is the use ...

Last Updated: 25 Nov 2015

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Detection of large deletion mutations in the SERPINC1 gene causing hereditary antithrombin deficiency by multiplex ligation-dependent probe amplification (MLPA).
 

Author(s): S-T Lee, H-J Kim, D-K Kim, R J L Schuit, S-H Kim

Journal: J. Thromb. Haemost.. 2008 Apr;6(4):701-3.

 

Last Updated: 14 Mar 2008

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[Hereditary antithrombin deficiency and pregnancy--what is the effective thromboprophylaxis?].
 

Author(s): Peter Majak, Florin Vikskjold, Ulrich Abildgaard

Journal: Tidsskr. Nor. Laegeforen.. 2003 Jan;123(2):144-6.

 

Last Updated: 27 Feb 2003

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Hereditary Antithrombin Deficiency" returned 1 free, full-text review articles on human participants. First 3 results:

[Hereditary antithrombin deficiency and hyperhomocysteinemia in venous thromboembolic disease].
 

Author(s): Zheng Xi-xi, Bing Zhong-xing, Liu Bao

Journal: Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2012 Dec;34(6):645-8.

 

Hypercoagulability state is the result of the interplay of genetic predisposition and risk factors. Many key enzymes and reactions in coagulation and anti-coagulation system are involved. Hereditary antithrombin deficiency is one of the major risk factors of venous thromboembolic ...

Last Updated: 4 Jan 2013

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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Safety, Pharmacokinetics and Efficacy of an AT-III Concentrate.
 

Status: Recruiting

Condition Summary: Antithrombin III Deficiency

 

Last Updated: 17 Feb 2014

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Atenativ Effect on Uterine Blood Flow and Preeclampsia
 

Status: Recruiting

Condition Summary: Antithrombin III Deficiency

 

Last Updated: 22 Mar 2016

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"Incidence and Consequences of Disorders of Glycosylation in Patients With Conotruncal and Septal Heart Defects"
 

Status: Recruiting

Condition Summary: Congenital Heart Diseases; Conotruncal Defects; Congenital Disorder of Glycosylation; Antithrombin III Deficiency

 

Last Updated: 21 Oct 2016

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