An Unusual Form of Chronic Neutropenia in a Father and Daughter with Hypogammaglobulinaemia
- 1 July 1977
- journal article
- research article
- Published by Wiley in British Journal of Haematology
- Vol. 36 (3) , 313-322
- https://doi.org/10.1111/j.1365-2141.1977.tb00654.x
Abstract
Chronic neutropenia, with an abundance of mature neutrophils in the bone marrow, was discovered in a father and daughter who also had common variable hypogammaglobulinemia. Under the stress of infection or following the administration of typhoid vaccine, release of neutrophils from the marrow was enhanced sufficiently to temporarily abolish neutropenia. Although their morphology was abnormal, the function of neutrophils in vitro was normal. The increased susceptibility to infection that characterized these patients appeared to be due primarily to their defect in humoral immunity rather than their neutropenia.This publication has 21 references indexed in Scilit:
- Heterogeneity of “Acquired” or Common Variable AgammaglobulinemiaNew England Journal of Medicine, 1974
- Metabolic and Bactericidal Activities of Human Eosinophils*British Journal of Haematology, 1971
- Ataxia telangiectasia with granulocytopeniaThe Journal of Pediatrics, 1970
- Pancreatic insufficiency and neutropenia with associated immunoglobulin deficitArchives of internal medicine (1960), 1970
- Chronic Neutropenia and Abnormal Cellular Immunity in Cartilage-Hair HypoplasiaNew England Journal of Medicine, 1970
- THE ENHANCEMENT OF BACTERIAL PHAGOCYTOSIS BY SERUMThe Journal of Experimental Medicine, 1969
- Quantitative Nitroblue Tetrazolium Test in Chronic Granulomatous DiseaseNew England Journal of Medicine, 1968
- Familial granulocytopenia and associated immunoglobulin abnormalityThe Journal of Pediatrics, 1967
- Chronic Idiopathic GranulocytopeniaNew England Journal of Medicine, 1964
- Myelokathexis — A New Form of Chronic GranulocytopeniaNew England Journal of Medicine, 1964