What is Antiphospholipid Syndrome and How Does It Affect You?

Understanding APS

Antiphospholipid syndrome is an autoimmune disorder where the immune system mistakenly attacks normal proteins in the blood. This leads to the formation of antiphospholipid antibodies, which can cause blood clots in veins and arteries. APS can manifest as a primary condition or alongside another autoimmune disease, such as systemic lupus erythematosus (SLE).

Common Symptoms

Symptoms of APS can vary but often include unexplained blood clots or pregnancy issues. Some might experience skin changes like a lacy rash, heart valve problems, or neurological symptoms such as memory loss. Women with APS may face challenges like miscarriages or preterm labor due to complications in pregnancy.

Risk Factors and Diagnosis

Several factors can increase the risk of developing APS, including having another autoimmune disease or a family history of blood clots. Diagnosing APS requires blood tests to detect the presence of antiphospholipid antibodies. These tests need to show positive results on two separate occasions, at least 12 weeks apart, to confirm the diagnosis.

Frequently Asked Questions

Key Takeaways

Understanding APS can help manage its complications and improve quality of life.

Related Articles

• How Do Doctors Diagnose Antiphospholipid Syndrome?
• What Increases Your Risk of Antiphospholipid Syndrome?
• How Can You Prevent Antiphospholipid Syndrome Complications?
• What Are the Telltale Symptoms of Antiphospholipid Syndrome?

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