May 18, · 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). Feb 04, · Evans syndrome is a rare disorder that causes the immune system to destroy certain blood cells. It can cause low blood cell levels and anemia, which may lead to a variety of symptoms. Treatments.
Oct 08, · Evans syndrome (ES) is a rare disease characterized by the simultaneous or sequential development of autoimmune hemolytic anemia (AIHA) and immune thrombocytopenia (ITP) and/or immune neutropenia. To better describe the characteristics and outcome of ES in adults, a survey was initiated in Cited by: Evans Syndrome A rare autoimmune disorder that is a combination of two or more immune hematological disorders in which the immune system destroys the body's red .
The life expectancy of Evans Syndrome depend on each case. The remissions of the disease are common, as well as relapses. While some people with Evans syndrome may have a normal life expectancy, others have more recurrences and exarberaciones of the disease which can shorten the hope of lives and reduce the quality of life. Jun 23, · Although usually considered a disease of children, adults are also be affected by Evans syndrome. It is generally a sporadic condition, and there are no genes identified to associate with the condition. It can rarely be inherited when it is called "familial Evans syndrome.".