Antithrombin III deficiency overview: Difference between revisions
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==Overview== | ==Overview== | ||
'''Antithrombin III deficiency''' is a [[rare disease|rare]] [[hereditary disorder]] that generally comes to light when a patient suffers recurrent venous [[thrombosis]] and [[pulmonary embolism]]. | '''Antithrombin III deficiency''' is a [[rare disease|rare]] [[hereditary disorder]] that generally comes to light when a patient suffers recurrent venous [[thrombosis]] and [[pulmonary embolism]]. Congenital antithrombin III deficiency is a genetic disorder that causes the blood to clot more than normal. | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
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[[CME Category::Cardiology]] | |||
[[Category:Disease]] | [[Category:Disease]] | ||
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[[Category:Cardiology]] | [[Category:Cardiology]] | ||
[[Category:Pediatrics]] | [[Category:Pediatrics]] | ||
Latest revision as of 21:46, 14 March 2016
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Antithrombin III deficiency Microchapters |
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Differentiating Antithrombin III deficiency from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Antithrombin III deficiency overview On the Web |
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American Roentgen Ray Society Images of Antithrombin III deficiency overview |
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Directions to Hospitals Treating Antithrombin III deficiency |
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Risk calculators and risk factors for Antithrombin III deficiency overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Antithrombin III deficiency is a rare hereditary disorder that generally comes to light when a patient suffers recurrent venous thrombosis and pulmonary embolism. Congenital antithrombin III deficiency is a genetic disorder that causes the blood to clot more than normal.