A NEW FORM OF PROLONGED TRANSIENT TYROSINEMIA PRESENTING WITH SEVERE METABOLIC ACIDOSIS
- 1 March 1975
- journal article
- Published by Wiley in Acta Paediatrica
- Vol. 64 (2) , 209-214
- https://doi.org/10.1111/j.1651-2227.1975.tb03823.x
Abstract
Danks, D. M., Tippett, P. and Rogers, J. (Genetics Research Unit, Royal Children's Hospital Research Foundation, Melbourne, Australia). A new form of prolonged transient tyrosinemia presenting with severe metabolic acidosis. Acta Paediatr Scand 64:209, 1975.–Yet another form of tyrosinemia is described, in a young baby who developed metabolic acidosis and ceased to grow when weaned from breast milk onto a higher protein formula. Severe tyrosyluria and mild tyrosinemia cleared on a low-protein diet which also corrected the acidosis. However, restoration of growth required a normal protein intake with very greatly reduced amounts of phenylalanine and tyrosine. The metabolic fault later resolved spontaneously at about 12 months of age. Mental development appears normal and liver disease was never apparent. The patient and her mother both excrete quite large quantities of an unidentified peptide.Keywords
This publication has 14 references indexed in Scilit:
- Biochemical Studies in a patient with “Tyrosinosis”**Australian and New Zealand Journal of Medicine, 1974
- DETECTION OF LIFE THREATENING INBORN ERRORS OF METABOLISM DURING INFANCYJournal of Paediatrics and Child Health, 1973
- Metabolic Studies in a Patient with Hepatic Cytosol Tyrosine Aminotransferase DeficiencyPediatric Research, 1971
- Neonatal Hepatitis in Premature Infants Simulating Hereditary TyrosinosisArchives of Disease in Childhood, 1971
- Biochemical Observations on So-called Hereditary TyrosinemiaPediatric Research, 1970
- Recovery after dietary treatment of an infant with features of tyrosinosis.Archives of Disease in Childhood, 1969
- HEREDITARY TYROSINEMIAActa Paediatrica, 1969
- Tyrosinosis. A study of 6 cases.Archives of Disease in Childhood, 1966
- Tyrosinemia: An inborn error of tyrosine metabolism with cirrhosis of the liver and multiple renal tubular defects (de Toni-Debré-Fanconi syndrome)The Journal of Pediatrics, 1965
- Automatic Recording Apparatus for Use in Chromatography of Amino AcidsAnalytical Chemistry, 1958