INHERITED DEFECT OF NEUTROPHIL MOBILITY IN SHWACHMAN SYNDROME

被引:90
作者
AGGETT, PJ
HARRIES, JT
HARVEY, BAM
SOOTHILL, JF
机构
[1] INST CHILD HLTH, DEPT IMMUNOL, 30 GUILFORD ST, LONDON WC1N 1EH, ENGLAND
[2] HOSP SICK CHILDREN, DEPT CHILD HLTH, LONDON WC1N 3JH, ENGLAND
关键词
D O I
10.1016/S0022-3476(79)80578-8
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Selected immunologic functions were assessed in 14 patients with the Shwachman syndrome. Nine patients were neutropenic and four had low levels of IgA or of IgM. Neutrophil mobility was significantly defective in the group of patients as a whole (in 12 it was below the lower limit of normal) and in their parents. No other consistent abnormality in immunity was found. These results suggest that the defective neutrophil mobility is a feature of Shwachman syndrome which may contribute to the vulnerability of these patients to frequent infections. The defect appears to be a primary genetic one, inherited as an autosomal recessive characteristic consistent with the assumed inheritance of Shwachman syndrome. © 1979 The C. V. Mosby Co.
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页码:391 / 394
页数:4
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