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used to treat
hereditary tyrosinemia type 1, a rare genetic disorder that prevents the body from breaking down the amino acid tyrosine, causing insufficient weight gain, jaundice, and liver and kidney failure.
Type 1 is the most severe form of tyrosinemia, with symptoms generally beginning in the first few months of life. While the dosage depends on each patient, most take 30 capsules of 20 mg each
month.
