Tyrosinemia: A rare genetic metabolic disorder characterized by a deficiency of particular enzymes which prevents the breakdown of tyrosine which then builds up in the liver.
More detailed information about the symptoms,
causes, and treatments of Tyrosinemia is available below.
Symptoms of Tyrosinemia
See full list of 26
symptoms of Tyrosinemia
Home Diagnostic Testing
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Wrongly Diagnosed with Tyrosinemia?
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Causes of Tyrosinemia
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Disease Topics Related To Tyrosinemia
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Less Common Symptoms of Tyrosinemia
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Misdiagnosis and Tyrosinemia
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Tyrosinemia: Research Doctors & Specialists
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Research about Tyrosinemia
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Clinical Trials for Tyrosinemia
The US based website ClinicalTrials.gov lists information on both federally
and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Tyrosinemia include:
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Statistics for Tyrosinemia
Tyrosinemia: Broader Related Topics
Types of Tyrosinemia
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Definitions of Tyrosinemia:
Autosomal recessive defect in tyrosine metabolism resulting in liver and kidney disturbances and mental retardation
- (Source - WordNet 2.1)
Tyrosinemia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Tyrosinemia, or a subtype of Tyrosinemia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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