BLOOD-TRANSFUSIONS IN THE THERAPY OF A CASE OF PROLIDASE DEFICIENCY

被引：22

作者：

BERARDESCA, E ^{[1
]}

FIDELI, D ^{[1
]}

BELLOSTA, M ^{[1
]}

DYNE, KM ^{[1
]}

ZANABONI, G ^{[1
]}

CETTA, G ^{[1
]}

机构：

[1] UNIV PAVIA,DEPT BIOCHEM,CTR STUDY CONNECT TISSUE DISORDERS,I-27100 PAVIA,ITALY

来源：

BRITISH JOURNAL OF DERMATOLOGY | 1992年 / 126卷 / 02期

关键词：

D O I：

10.1111/j.1365-2133.1992.tb07820.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

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.

引用

页码：193 / 195

页数：3

共 4 条

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[2]

JACKSON SH, 1975, CAN MED ASSOC J, V113, P759

[3] PROLIDASE DEFICIENCY IN 2 SIBLINGS WITH CHRONIC LEG ULCERATIONS - CLINICAL, BIOCHEMICAL, AND MORPHOLOGICAL ASPECTS [J].

LEONI, A ;

CETTA, G ;

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[4]

McKusick V. A., 1986, MENDELIAN INHERITANC

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