Triose phosphate isomerase deficiency: Report of a family
- 1 May 1986
- journal article
- research article
- Published by Wiley in Journal of Paediatrics and Child Health
- Vol. 22 (2) , 135-137
- https://doi.org/10.1111/j.1440-1754.1986.tb00205.x
Abstract
Triose phosphate isomerase (TPI) deficiency is associated with a syndrome of congenital non-spherocytic haemolytic anaemia, mental subnormality, motor impairmet, growth failure and cardiac failure. The deficiency state is characterized by moderately reduced red cell TPI activity, and marked instability of the abnormal enzyme to heat. The clinical features of an affected child are described, and some problems in the laboratory diagnosis delineated.Keywords
This publication has 5 references indexed in Scilit:
- Triose phosphate isomerase deficiency: Prenatal diagnosisThe Journal of Pediatrics, 1985
- Elevated Frequency of Carriers for Triosephosphate Isomerase Deficiency in Newborn InfantsPediatric Research, 1982
- Hereditary deficiency of triosephosphate isomerase in four unrelated familiesEuropean Journal of Clinical Investigation, 1979
- Genetic and non-genetic variation of triose phosphate isomerase isozymes in human tissuesAnnals of Human Genetics, 1973
- Hereditary Hemolytic Anemia with Triosephosphate Isomerase DeficiencyNew England Journal of Medicine, 1965