Hereditary Antithrombin Deficiency
Common Name(s)
Hereditary Antithrombin Deficiency
Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Hereditary Antithrombin Deficiency" for support, advocacy or research.
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Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Hereditary Antithrombin Deficiency" for support, advocacy or research.
Recommended Apps
Anonymously share and see how your answers compare with others with this condition while privately providing key pieces of information to medical researchers, disease advocacy groups, and others ONLY YOU select to help speed up cures and better alternatives.
Finding the right clinical trial for Hereditary Antithrombin Deficiency can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.
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:
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 ...
Journal: J. Thromb. Haemost.. 2008 Apr;6(4):701-3.
Journal: Tidsskr. Nor. Laegeforen.. 2003 Jan;123(2):144-6.
To view other free, full-text articles on human participants, please click on the link below.
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:
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 ...
To view other free, full-text review articles on human participants, please click on the link below.
Symptoms, Diagnosis, and Treatment
https://ghr.nlm.nih.gov/gene/SERPINC1
https://ghr.nlm.nih.gov/condition/hereditary-xanthinuria
https://ghr.nlm.nih.gov/condition/hereditary-angioedema
https://ghr.nlm.nih.gov/condition/hereditary-fructose-intolerance
https://ghr.nlm.nih.gov/condition/spastic-paraplegia-type-7
https://ghr.nlm.nih.gov/condition/protein-s-deficiency
https://ghr.nlm.nih.gov/primer/dtcghrpages
https://ghr.nlm.nih.gov/condition/tyrosinemia
https://ghr.nlm.nih.gov/condition/hereditary-pancreatitis
https://ghr.nlm.nih.gov/condition/complement-factor-i-deficiency
https://ghr.nlm.nih.gov/condition/protein-c-deficiency
https://ghr.nlm.nih.gov/condition/dihydropyrimidine-dehydrogenase-deficiency
https://ghr.nlm.nih.gov/condition/mevalonate-kinase-deficiency
https://ghr.nlm.nih.gov/condition/aceruloplasminemia
https://ghr.nlm.nih.gov/condition/factor-v-deficiency
https://ghr.nlm.nih.gov/condition/fumarase-deficiency
https://ghr.nlm.nih.gov/condition/hereditary-spherocytosis
https://ghr.nlm.nih.gov/condition/hereditary-hyperekplexia
https://ghr.nlm.nih.gov/condition/hereditary-hemochromatosis
There are currently no related results available in GeneReviews.
There are currently no related results available in Genetic Testing Registry.
Clinical Trial Information This information is provided by ClinicalTrials.gov
Condition Summary: Congenital Heart Diseases; Conotruncal Defects; Congenital Disorder of Glycosylation; Antithrombin III Deficiency
Condition Summary: Antithrombin Deficiency Type 2
Finding the right clinical trial for Hereditary Antithrombin Deficiency can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.