TREATMENTS &
RESEARCH

Search the
latest
treatment
information
here.

Dr. Huntley's
Diagnosis
Checklist

Have a symptom?
See what questions
a doctor would ask.
 

What is Immune Thrombocytopenic Purpura?



What is Immune Thrombocytopenic Purpura?

  • Immune Thrombocytopenic Purpura: Reduced blood platelets causing visible skin blemishes from bleeding or bruising.
  • Immune Thrombocytopenic Purpura: Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms.
    Source - Diseases Database

Immune Thrombocytopenic Purpura is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Immune Thrombocytopenic Purpura, or a subtype of Immune Thrombocytopenic Purpura, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Name and Aliases of Immune Thrombocytopenic Purpura

Main name of condition: Immune Thrombocytopenic Purpura

Other names or spellings for Immune Thrombocytopenic Purpura:

ITP

Werlhof disease, Idiopathic thrombocytopenic purpura Source - Diseases Database

Idiopathic thrombocytopenic purpura, Thrombocytopenic purpura, autoimmune, Autoimmune thrombocytopenic purpura
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Types of Immune Thrombocytopenic Purpura:

Subtypes of Immune Thrombocytopenic Purpura: Idiopathic Immune Thrombocytopenic Purpura, Secondary Immune Thrombocytopenic Purpura, Acute thrombocytopenic purpura, Chronic thrombocytopenic purpura
Parent types of Immune Thrombocytopenic Purpura: Autoimmune diseases, Blood conditions, Purpura

Organs Affected by Immune Thrombocytopenic Purpura:

blood

How many people get Immune Thrombocytopenic Purpura?

Prevalance of Immune Thrombocytopenic Purpura: rare.

Who gets Immune Thrombocytopenic Purpura?

Patient Profile for Immune Thrombocytopenic Purpura: Acute ITP more common in children, often after a virus. Chronic ITP more common in adults.
Gender Profile for Immune Thrombocytopenic Purpura: Acute ITP equally boys or girls; chronic ITP more common in women 2-1 than men.

How serious is Immune Thrombocytopenic Purpura?

Prognosis of Immune Thrombocytopenic Purpura: Acute ITP: 85% of children recover within 1 year and have no remissions.
Complications of Immune Thrombocytopenic Purpura: see complications of Immune Thrombocytopenic Purpura

What causes Immune Thrombocytopenic Purpura?

Class of Condition for Immune Thrombocytopenic Purpura: autoimmune
Causes of Immune Thrombocytopenic Purpura: see causes of Immune Thrombocytopenic Purpura

Can anyone else get Immune Thrombocytopenic Purpura?

Contagion of autoimmunity: generally not; see details in contagion of autoimmune diseases.

How is it treated?

Doctors and Medical Specialists for Immune Thrombocytopenic Purpura: Hematologists ; see also doctors and medical specialists for Immune Thrombocytopenic Purpura.
Treatments for Immune Thrombocytopenic Purpura: see treatments for Immune Thrombocytopenic Purpura


 » Next page: Online Medical Textbooks for Immune Thrombocytopenic Purpura

Medical Tools & Articles:


Next articles:

Tools & Services:

Medical Articles:

Forums & Message Boards

Major Disease Research

Research
symptoms, treatments,
and misdiagnosis
of major diseases.

Multiple Symptom
Checker

Check one
or many
symptoms
 
By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.