Immune Thrombocytopenic Purpura
Description
Immune thrombocytopenic purpura (or immune thrombocytopenia; ITP) is an autoimmune coagulation disorder characterized by isolated thrombocytopenia (a platelet count <100,000/microL), in the absence of any underlying disorder that may be associated with thrombocytopenia.
Clinical Features
Top most frequent phenotypes and symptoms related to Immune Thrombocytopenic Purpura
- Immunodeficiency
- Thrombocytopenia
- Autoimmunity
- Bruising susceptibility
- Hematuria
- Abnormal bleeding
- Gastrointestinal hemorrhage
- Epistaxis
- Purpura
- Cerebral hemorrhage
And another 6 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Based on the latest data available IMMUNE THROMBOCYTOPENIC PURPURA have a estimated prevalence of 25 per 100k worldwide.— No data available about the known clinical features onset.
Alternative names
Immune Thrombocytopenic Purpura Is also known as idiopathic thrombocytopenic purpura, immune thrombocytopenia, immune thrombocytopenic purpura, thrombocytopenic purpura, autoimmune, itp.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Sources and references
You can check the following sources for additional information.
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