Idiopathic thrombocytopenia purpura (ITP)

Idiopathic thrombocytopenic purpura

Idiopathic
Idiopathic thrombocytopenic purpura (ITP) is the condition of having an abnormally low platelet count of no known cause. As most incidents of ITP appear to be related to the production of antibodies against platelets, immune thrombocytopenic purpura or immune thrombocytopenia are terms also used to describe this condition. Often ITP is asymptomatic (devoid of obvious symptoms), however a very low platelet count can lead to visible symptoms, such as purpura (large bruises), or more seriously, bleeding diathesis. ITP was first described by the German physician Paul Gottlieb Werlhof in 1735, and was originally referred to as Werlhof’s disease...

Idiopathic thrombocytopenia purpura (ITP) - List of case studies

Chromosome 22 micro-deletion syndrome

include childhood rheumatoid arthritis (JRA), idiopathic thrombocytopenia purpura (ITP), thyroid dysfunction, vitiligo, hemolytic anemia, autoimmune ...

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