Liver

Clotting of the blood in the liver can sometimes be under-diagnosed in APS, and is usually detected by the findings of abnormal liver function tests.

Recurrent clotting can occasionally lead to cirrhosis of the liver and, in rare, untreated cases, serious clotting of the liver veins can occur leading to more severe liver damage – a condition known as Budd Chiari syndrome. With this condition, the blood clots can prevent blood from flowing out of the liver and symptoms can include nausea, vomiting, jaundice (yellow skin), dark urine and swelling of the abdomen.

Early diagnosis and anticoagulation treatment generally leads to improvement of the milder forms of liver involvement.

Diagnosis and treatment

APS is usually diagnosed from a combination of a positive blood test and symptoms. If you are under 50 and have suffered a thrombosis, or have had more than one pregnancy loss, you should discuss with your doctor whether you need blood tests.

Related conditions

Some people with APS will also have other autoimmune conditions, as may their family members. APS has been linked with many other autoimmune conditions, including rheumatoid arthritis, lupus, Raynaud’s phenomenon, and Sjögren’s syndrome.

Newly diagnosed

Receiving a new diagnosis of APS can be frightening, and no doubt you will want to know exactly what APS is. Following this, you will likely have a great many more questions to ask about the condition and how it can affect you. We are here to help!

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Our mission is to achieve earlier diagnosis and offer support to anyone affected by antiphospholipid syndrome (APS) through awareness, education and research.

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