Article

Molecular and cellular characterization of congenital dyserythropoietic anaemia type 1

2009-01-01

Abstract excerpt

Congenital dyserythropoietic anaemia type I (CDA I) is an autosomal recessive disorder of erythropoiesis characterized by a clinical picture of anaemia secondary to ineffective erythropoiesis, haemolysis and striking morphology of erythroid precursors (internuclear chromatin bridges, spongy heterochromatin, invaginations of nuclear membrane) and erythrocytes (macrocytosis, anisocytosis, basophilic stippling) in th...

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Literature Corpus work: 47625f44-f7d0-5f21-8a8d-4da5dfbb6ec6
DOI: 10.21954/ou.ro.00010035

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