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References in periodicals archive ?
Antiphospholipid syndrome, also known as APAS or APS, is an autoimmune disorder where a person experiences a higher risk of blood clots.
Key words: Renal biopsy, antiphospholipid syndrome nephropathy, lupus nephritis, thrombotic microangiopathy, systemic lupus erythematosus.
We analyzed the large amount of data generated by GT, based on the search term "antiphospholipid" in a 5-year worldwide web-based research (from January 2012 to January 201/).
Patients with APS show persistently positive antiphospholipid antibodies (aPLs), which belong to a group of heterogeneous autoimmune antibodies recognizing and attacking phospholipid-binding proteins.
We hypothesize that the patient's history of SLE, antiphospholipid syndrome, and prolonged steroid use in the past 14 years contributed to his advanced atherosclerotic disease.
Moreover, they examined maternal and perinatal complications in this population, antiphospholipid antibody status, pregnancy complications, and the total number of live births from SLE patients.
As per the International Consensus Guidelines, the definite diagnosis of CAPS requires four criteria to be fulfilled: (1) involvement of three or more organs/tissues, (2) development of manifestations simultaneously or within one week, (3) histologic evidence of vascular thrombosis, and (4) laboratory confirmation of presence of antiphospholipid antibodies [6].
As widespread thrombosis is the key feature of TS, it brings this syndrome closer to other clinical entities known for hypercoagulable states and extensive thrombotic events like Antiphospholipid Syndrome (APS), Protein C and S Deficiency [3], Factor V Leiden, Heparin Induced Thrombocytopenia (HIT), Thrombocytopenic Purpura (TTP), and Hemolysis Elevated Liver enzymes and Low Platelets (HELLP) syndrome.
We present a case with antiphospholipid antibody syndrome (APS) who developed recurrent nephrotic syndrome (NS) 6 years apart.
The causes of splenic infarction are cardiogenic emboli such as atrial fibrillation, autoimmune diseases such as antiphospholipid syndrome, hematological diseases, and infection.
Antiphospholipid antibodies were retested 6 weeks later and were all negative.
The differential diagnosis of DAH is broad and includes medications, coagulopathy, illicit drugs, and other autoimmune diseases including systemic vasculitis, good pastures syndrome, and antiphospholipid antibody syndrome.