[tahy-roh-si-nee-mee-uh, tir-oh-]
noun Pathology.
an inherited disorder of tyrosine metabolism that can lead to liver and kidney disease and mental retardation unless controlled by a special diet.

1960–65; tyrosine + -emia

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Medical Dictionary

tyrosinemia ty·ro·si·ne·mi·a (tī'rə-sĭ-nē'mē-ə)
An inherited disorder of tyrosine metabolism marked by an increase in the concentration of tyrosine in the blood, an increase in urinary excretion of tyrosine and related compounds, hepatosplenomegaly, nodular cirrhosis of the liver, multiple renal tubular reabsorptive defects, and vitamin D-resistant rickets.

The American Heritage® Stedman's Medical Dictionary
Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.
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Encyclopedia Britannica


inherited inability of the body to metabolize normally the amino acid tyrosine. In the normal metabolic pathway of tyrosine, para-(p-)hydroxyphenylpyruvic acid is converted to homogentisic acid (in the liver) by a specific organic catalyst or enzyme, called p-hydroxyphenylpyruvic acid oxidase. This enzyme is not active in individuals with tyrosinemia. Clinical features of the disease include an increase in concentration of tyrosine in the blood and urine, defects in kidney function, and replacement of liver cells with fibrous tissue. There may also be fewer circulating platelets in the blood than normal and an increased pigmentation of the skin. Affected children may develop a form of rickets that does not improve with administration of vitamin D. A diet low in tyrosine and phenylalanine, an amino acid that the body converts to tyrosine, helps keep tyrosinemia under control. This disorder is extremely rare; it is transmitted through a recessive gene.

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Encyclopedia Britannica, 2008. Encyclopedia Britannica Online.
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