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Recurrent sepsis with deficiencies of C2 and galactokinase.

作者信息

Borzy M S, Wolff L, Gewurz A, Buist N R, Lovrien E

出版信息

Am J Dis Child. 1984 Feb;138(2):186-91. doi: 10.1001/archpedi.1984.02140400068017.

DOI:10.1001/archpedi.1984.02140400068017
PMID:6695877
Abstract

A 4-year-old girl with recurrent, severe bacterial infections and absence of both the second component of complement and galactokinase was investigated for immunodeficiency. The C2 deficiency (C2D) was diagnosed after four major pyogenic infections. Results of studies of cellular and humoral immunity were normal, as were polymorphonuclear leukocyte chemotaxis and bactericidal activities and alternative-pathway hemolytic activity. Serum chemotactic and opsonic activities were deficient in this patient and in an older, asymptomatic sibling with C2D. Fresh-frozen plasma, administered during an episode of Streptococcus pneumoniae meningitis, enhanced serum opsonic activity at 12 hours after infusion. To our knowledge, this is the first description of C2D in a patient with a documented second, unusual genetic defect.

摘要

相似文献

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引用本文的文献

1
Clinical features of galactokinase deficiency: a review of the literature.半乳糖激酶缺乏症的临床特征:文献综述
J Inherit Metab Dis. 2002 Dec;25(8):629-34. doi: 10.1023/a:1022875629436.
2
Defective activation of the alternative pathway of complement in patients with homozygous C2 deficiency: studies in two unrelated families.纯合子C2缺乏症患者补体替代途径的激活缺陷:对两个无关家族的研究。
Eur J Pediatr. 1991 Jul;150(9):647-51. doi: 10.1007/BF02072626.
3
Infectious diseases associated with complement deficiencies.与补体缺陷相关的传染病。
Clin Microbiol Rev. 1991 Jul;4(3):359-95. doi: 10.1128/CMR.4.3.359.