| Literature DB >> 2049466 |
Abstract
A child is described who suffered from a severe congenital anemia. The anemia persisted and a regular transfusional regimen became necessary. Bone marrow aspirates showed an erythroblastic hyperplasia associated with some dyserythropoietic features. A most striking and constant finding was the presence of many inter-erythroblastic chromatin bridges. The reticulocyte count was always low, in spite of the increased erythropoietic activity. A beta-thalassemia trait inherited from the mother was demonstrated. The hypothesis of dyserythropoiesis/thalassemia syndrome was put forward, based on the assumption that the two genes may have interacted with each other.Entities:
Mesh:
Substances:
Year: 1991 PMID: 2049466 DOI: 10.1007/bf01703146
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673