Tyrosinosis
National Institutes of Health
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Richner-Hanhart's syndrome correspond to an hypertyrosinemia due to a deficiency of a soluble tyrosine amino-transferase. This…
Twenty infants and young children with hereditary fructose intolerance (HFI) were admitted to hospital. None was diagnosed at…
A case of tyrosinosis due to lack of soluble tyrosine aminotransferase is described. The first clinical sign of this disorder may…
Summary: An adult mentally retarded patient with tyrosinaemia and tyrosyluria is described. The absence of renal and hepatic…
Three premature infants are reported who developed obstructive jaundice in the first 3 months of life, with a chemical and…
TYROSINOSIS is a hereditary disorder characterized by cirrhosis, severe hypophosphatemic rickets, renal tubular defects, and…
IN TYROSINEMIA or tyrosinosis1the main clinical features are multiple renal tubular defects as in the typical de ToniDebre…
FOUR patients with "tyrosinosis" were brought to our attention and investigated during the past year. All of them came from the…
not improved by operation further emboli occurred in two, and two had emboli for the first time during the follow-up years. Three…