Documents TYPE II TYROSINEMIA

WHAT IS TYPE II TYROSINEMIA? Type II tyrosinemia is an inborn error of tyrosine metabolism caused by a deficient activity of the enzyme tyrosine aminotransferase (TAT). As

Documents Richner-Hanhart Syndrome (Tyrosinemia Type II)

To the Editor: Richner-Hanhart syndrome, also known as tyrosinemia type II or oculocutaneous tyrosinemia, is a rare autosomal- recessive, childhood-onset, metabolic hereditary

Documents Hepatic Enzymes of Tyrosine Metabolism in Tyrosinemia II

Hepatic Enzymes of Tyrosine Metabolism in Tyrosinemia IIVol. 73, No.6 Printed in U.S.A. Hepatic Enzymes of Tyrosine Metabolism in Tyrosinemia II LOWELL A. GOLDSMITH, MD,