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TAR syndrome

TAR syndrome: Introduction

TAR syndrome: A rare genetic disorder characterized by the absence of radial bones of both forearms and thrombocytopenia. More detailed information about the symptoms, causes, and treatments of TAR syndrome is available below.

Symptoms of TAR syndrome

Home Diagnostic Testing

Home medical testing related to TAR syndrome:

Wrongly Diagnosed with TAR syndrome?

TAR syndrome: Related Patient Stories

TAR syndrome: Complications

Review possible medical complications related to TAR syndrome:

Causes of TAR syndrome

Read more about causes of TAR syndrome.

Disease Topics Related To TAR syndrome

Research the causes of these diseases that are similar to, or related to, TAR syndrome:

Less Common Symptoms of TAR syndrome

Misdiagnosis and TAR syndrome

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TAR syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for TAR syndrome

Medical research articles related to TAR syndrome include:

Click here to find more evidence-based articles on the TRIP Database

TAR syndrome: Animations

Research about TAR syndrome

Visit our research pages for current research about TAR syndrome treatments.

Statistics for TAR syndrome

TAR syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about TAR syndrome, or answer someone else's question, on our message boards:

Definitions of TAR syndrome:

TAR syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that TAR syndrome, or a subtype of TAR syndrome, 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 TAR syndrome as a "rare disease".
Source - Orphanet

 

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