Antiphospholipid syndrome classification: Difference between revisions
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==Classification== | ==Classification== | ||
*Antiphospholipid syndrome (APS) can be divided into primary and secondary APS based on the underlying etiology. In primary APS, no underlying disease in associated with the syndrome. Whereas, secondary APS is associated with an underlying autoimmune disorder. | *Antiphospholipid syndrome (APS) can be divided into primary and secondary APS based on the underlying etiology. In primary APS, no underlying disease in associated with the syndrome. Whereas, secondary APS is associated with an underlying [[Autoimmune disease|autoimmune]] disorder. | ||
==References== | ==References== |
Latest revision as of 15:54, 24 April 2018
Antiphospholipid syndrome Microchapters |
Differentiating Antiphospholipid syndrome from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Antiphospholipid syndrome classification On the Web |
American Roentgen Ray Society Images of Antiphospholipid syndrome classification |
Risk calculators and risk factors for Antiphospholipid syndrome classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Feham Tariq, MD [2]
Overview
- Antiphospholipid syndrome (APS) can be divided into primary and secondary APS.
Classification
- Antiphospholipid syndrome (APS) can be divided into primary and secondary APS based on the underlying etiology. In primary APS, no underlying disease in associated with the syndrome. Whereas, secondary APS is associated with an underlying autoimmune disorder.