PMID: 3769984Aug 1, 1986Paper

A variant of the congenital dyserythropoietic anaemia type II with structural abnormalities in the granulocytic series

European Journal of Pediatrics
C VermylenG Cornu

Abstract

Typical features of congenital dyserythropoietic anaemia (CDA) were found in a 13-year-old girl admitted for chronic recurrent multifocal osteomyelitis. The findings on light microscopy were in agreement with those described in CDA type II, whereas on electron microscopy, the ultrastructure findings were compatible with both types I and II. The acidified serum lysis test (Ham test) performed with eight normal sera was negative. The patient's red blood cells showed an increased agglutinability with anti-i antibodies. Morphological changes were also shown in the mature neutrophilic granulocyte suggesting that the primary disorder exists already in the multipotent stem cell.

References

Apr 1, 1970·British Journal of Haematology·S M LewisJ V Dacie
Aug 1, 1970·Journal of Cellular Physiology·B L Pike, W A Robinson

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Citations

Oct 16, 1999·British Journal of Haematology·A Beauchamp-NicoudJ Delaunay
Oct 18, 2011·Journal of Infection and Public Health·Nevio Cimolai
Jan 1, 1996·American Journal of Hematology·P W Marks, A J Mitus
Mar 3, 2007·Arthritis and Rheumatism·Zakiya S Al-MosawiPolly J Ferguson
Jun 1, 1993·Baillière's Clinical Haematology·M N Fukuda

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