Tyrosinemia Support Group
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provenahelp
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Tyrosinemia Information
Tyrosinemia (or "Tyrosinaemia") is an error of metabolism, usually inborn, in which the body can not effectively break down the amino acid tyrosine, found in most animal and plant proteins. Tyrosinemia is inherited in an autosomal recessive pattern. There are three types of tyrosinemia, each with distinctive symptoms and caused by the deficiency of a different enzyme. Treatment varies depending on the specific type. A low protein diet may be required in the management of tyrosinemia.
See more Tyrosinemia Information.


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