Volume 22, Issue 2 pp. 135-137
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Triose phosphate isomerase deficiency: Report of a family

ARTHUR C. L. CLARK

Corresponding Author

ARTHUR C. L. CLARK

Department of Paediatrics, Monash University, Melbourne, Australia

Dr A. C. L. Clark, Department of Paediatrics, Queen Victoria Medical Centre, 172 Lonsdale Street, Melbourne 3000, Australia.Search for more papers by this author
MARGARET A. SZOBOLOTZKY

MARGARET A. SZOBOLOTZKY

Department of Paediatrics, Monash University, Melbourne, Australia

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First published: May 1986
Citations: 1

A. C. L. Clark, MD, FRACP, M. A. Szobolotzky, BSc.

Abstract

Triose phosphate isomerase (TPI) deficiency is associated with a syndrome of congenital non-spherocytic haemolytic anaemia, mental subnormality, motor impairment, 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.

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