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
See full list of 27
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
See full list of 23
occasional symptoms of TAR syndrome
Misdiagnosis and TAR syndrome
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Read more about Misdiagnosis and TAR syndrome
TAR syndrome: Research Doctors & Specialists
Research related physicians and medical specialists:
- Blood Health Specialists (Hematology):
- Arthritis & Joint Health Specialists (Rheumatology):
- more specialists...»
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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
More TAR syndrome animations & videos
Research about TAR syndrome
Visit our research pages for current research about TAR syndrome treatments.
Statistics for TAR syndrome
TAR syndrome: Broader Related Topics
Types of TAR syndrome
User Interactive Forums
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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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