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https://rarediseases.info.nih.gov/diseases/6389/evans-syndrome
May 18, 2016 · Evans syndrome is a very rare autoimmune disorder in which the immune system destroys the body's red blood cells, white blood cells and/or platelets.Affected people often experience thrombocytopenia (too few platelets) and Coombs' positive hemolytic anemia (premature destruction of red blood cells).Signs and symptoms may include purpura, paleness, fatigue, and light-headedness.
https://www.aarda.org/diseaseinfo/evans-syndrome/
Evans syndrome is a very rare autoimmune disorder in which the immune system destroys the body’s red blood cells, white blood cells and/or platelets. Affected people often experience thrombocytopenia (too few platelets) and Coombs’ positive hemolytic anemia (premature destruction of red blood cells). Signs and symptoms may include purpura, paleness, fatigue, and light-headedness.
https://www.verywellhealth.com/evans-syndrome-4011862
Apr 14, 2019 · Evans Syndrome is a combination of two or more immune hematological disorders where your immune system attacks your white blood cells, red blood cells and/or platelets. These include immune thrombocytopenia (ITP), autoimmune hemolytic anemia (AIHA), and/or autoimmune neutropenia (AIN). These diagnoses might occur at the same time but can also ...
https://rarediseases.info.nih.gov/diseases/6389/evans-syndrome/cases/57655
Jul 28, 2016 · The exact cause of Evans syndrome is not known; however, it is known that Evans syndrome is a disorder of the immune system.The immune system is a network of cells, tissues, and organs that work together to defend the body against germs (foreign substances). The immune system normally responds to foreign substances by producing specialized proteins, called antibodies, that …
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3879039/
Introduction. Evans syndrome (ES) is a rare hematological disease commonly defined by the combination of simultaneous or sequential autoimmune hemolytic anemia (AIHA) and immune thrombocytopenia (ITP) sometimes associated with neutropenia in the absence of known underlying etiology.Cited by: 4
https://en.wikipedia.org/wiki/Evan%27s_syndrome
Evans syndrome is an autoimmune disease in which an individual's immune system attacks their own red blood cells and platelets, the syndrome can include immune neutropenia. These immune cytopenias may occur simultaneously or sequentially. Its overall phenotype resembles a combination of autoimmune hemolytic anemia and immune thrombocytopenic purpura. ...Specialty: Hematology
https://contact.org.uk/advice-and-support/medical-information/conditions/e/evans-syndrome/
Background. Evans' syndrome is a rare autoimmune condition (where the immune system attacks the body's own cells). In this condition, the body makes antibodies that destroy the red blood cells, platelets (small bodies within the blood that help it clot) and white blood cells (which help fight off infection).
http://williams.medicine.wisc.edu/evanssyndrome.pdf
Keywords: Evans syndrome, autoimmune cytopenias, auto-immune thrombocytopenia, autoimmune haemolytic anaemia, immunosuppression. Evans syndrome is defined by the combination (either simultaneously or sequentially) of autoimmune haemolytic anaemia (AIHA) and immune thrombocytopenia (ITP), sometimes together with immune neutropenia, in the absence
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2753340/
Hereditary spherocytosis (HS) is a genetic disorder of the red blood cell membrane clinically characterized by anemia, jaundice and splenomegaly. Evans' syndrome is a clinical syndrome characterized by autoimmune hemolytic anemia (AIHA) accompanied by immune thrombocytopenic purpura (ITP). It results from a malfunction of the immune system that ...Cited by: 2
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