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Genetic Risk Factors Associated With Antiphospholipid Antibody Syndrome
Sponsor: Duke University
Summary
Antiphospholipid antibody syndrome (APS) is characterized by the presence of antiphospholipid antibodies, which are proteins in the blood that interfere with the body's ability to perform normal blood clotting. Clinical problems associated with antiphospholipid antibodies include an increased risk for the formation of blood clots in the lungs or deep veins of the legs, stroke, heart attack, and recurrent miscarriages. It is possible that some people with APS have a genetic predisposition for developing the syndrome. This study will use a genetic strategy to identify potential inherited risk factors for the development of APS by recruiting people with APS who have family members also affected by the syndrome or by another autoimmune disorder, such as lupus or rheumatoid arthritis.
Official title: Genetics of Antiphospholipid Antibody Syndrome
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
2800
Start Date
2006-06
Completion Date
2028-03
Last Updated
2025-03-19
Healthy Volunteers
No
Conditions
Locations (1)
Duke University Medical Center
Durham, North Carolina, United States