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.

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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.

OMIM ORPHANET Rare Disease Search Engine

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