Blood transfusions in the therapy of a case of prolidase deficiency
- 1 February 1992
- journal article
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 126 (2) , 193-195
- https://doi.org/10.1111/j.1365-2133.1992.tb07820.x
Abstract
A case is reported of a 15-year-old boy with prolidase deficiency and marked urinary excretion of the iminodipeptide gly-pro. Prolidase activity of erythrocytes against substrate glycyl-proline was deficient, but after blood transfusions this was increased to 15.7% of donor activity and declined to 12% and 3.4% of normal activity after 8 and 45 days, respectively. Urinary iminodipeptide levels following transfusion remained unaltered.Keywords
This publication has 2 references indexed in Scilit:
- Prolidase deficiency in two siblings with chronic leg ulcerations. Clinical, biochemical, and morphologic aspectsArchives of Dermatology, 1987
- Clinical and biochemical characteristics of prolidase deficiency in siblingsAmerican Journal of Medical Genetics, 1984