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Pathway Description
Tyrosinemia Type 3 (TYRO3)
Homo sapiens
Category:
Metabolite Pathway
Sub-Category:
Disease
Created: 2022-11-01
Last Updated: 2023-10-25
Tyrosinemia type 3, one of the three types of tyrosinemia, is a rare disorder with only a few reported cases. Tyrosinemia type 3 results from a defect in the HPD gene which codes for 4-hydroxyphenylpyruvate dioxygenase. 4-Hydroxyphenylpyruvate dioxygenase plays a role in the catabolism of tyrosine by catalyzing the conversion of 4-hydroxyphenylpyruvate to homogentisate. A defect in this enzyme causes tyrosine and phenylalanine to accumulate in the blood resulting in increased excretion of tyrosine in the urine. Tyrosinemia type 3 symptoms include: seizures, mental retardation and intermittent ataxia (occasional loss of balance and coordination).
References
Tyrosinemia Type 3 (TYRO3) References
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Pubmed: 10049785
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