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What is Thrombocytopenia -- chromosome breakage?

What is Thrombocytopenia -- chromosome breakage?

  • Thrombocytopenia -- chromosome breakage: A very rare inherited disorder characterized by low blood platelets, carcinomas and autoimmunity.

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

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Thrombocytopenia -- chromosome breakage as a "rare disease".
Source - Orphanet

Thrombocytopenia -- chromosome breakage: Introduction

Types of Thrombocytopenia -- chromosome breakage:

Broader types of Thrombocytopenia -- chromosome breakage:

What causes Thrombocytopenia -- chromosome breakage?

Causes of Thrombocytopenia -- chromosome breakage: see causes of Thrombocytopenia -- chromosome breakage

What are the symptoms of Thrombocytopenia -- chromosome breakage?

Symptoms of Thrombocytopenia -- chromosome breakage: see symptoms of Thrombocytopenia -- chromosome breakage

Thrombocytopenia -- chromosome breakage: Testing

Diagnostic testing: see tests for Thrombocytopenia -- chromosome breakage.

Misdiagnosis: see misdiagnosis and Thrombocytopenia -- chromosome breakage.

How is it treated?

Doctors and Medical Specialists for Thrombocytopenia -- chromosome breakage: Hematologist, Medical Geneticist ; see also doctors and medical specialists for Thrombocytopenia -- chromosome breakage.
Treatments for Thrombocytopenia -- chromosome breakage: see treatments for Thrombocytopenia -- chromosome breakage

Name and Aliases of Thrombocytopenia -- chromosome breakage

Main name of condition: Thrombocytopenia -- chromosome breakage

Other names or spellings for Thrombocytopenia -- chromosome breakage:

Helmerhorst-Heaton-Crosson syndrome, Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage, Thrombocytopenia 2, THC2, Thrombocytopenia, autosomal dominant, Helmerhorst Heaton Crossen syndrome

Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage, Helmerhorst Heaton Crossen syndrome, THC2, Thrombocytopenia 2, Thrombocytopenia, autosomal dominant
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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