HEREDITARY DEFICIENCY OF PEROXIDASE AND PHOSPHOLIPIDS IN EOSINOPHILIC GRANULOCYTES

被引:19
作者
PRESENTEY, B
SZAPIRO, L
机构
[1] Haematological Department Department of Pediatrics, Health Insurance Institution Kupat Holim, Rehovoth
关键词
D O I
10.1159/000208873
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A family with a hereditary deficiency of peroxidase and phospholipids of the eosinophilis is described. The defect is not accompanied by any morphological anomalies. Its mode of inheritance is autosomal and recessive. No connection between this defect and any form of illness has been found. All cases of this anomaly discovered to date were of Yemenite origin. © 1969 S. Karger AG, Basel.
引用
收藏
页码:359 / +
页数:1
相关论文
共 6 条
[1]  
GRAHAMKNOLL, 1952, PLANCHES HEMATOLOGIE
[2]  
LISON, 1952, PLANCHES HEMATOLOGIE
[3]  
OSGOOD, 1958, CARTWRIGHT DIAGNOSTI, P91
[4]  
PRESENTEY B, 1969, AM J CLIN PATHOL, V51, P451
[5]   A NEW ANOMALY OF EOSINOPHILIC GRANULOCYTES [J].
PRESENTEY, BZ .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1968, 49 (06) :887-+
[6]  
PRESENTEY BZ, 1969, AM J CLIN PATHOL, V51, P458