δβ-Thalassemia results from the deletion of both δ and βgenes. Homozygotes for δβ-thalassemia have 100% HbF and, because of the increased synthesis of HbF, may have thalassemia …

Co-inheritance of deletional and non-deletional alpha (alpha) thalassaemias may result in various thalassaemia syndromes. Concomitant co-inheritance with beta (beta) and delta (delta) gene …

Thalassemia and the Kleihauer-Betke test. Thalassemia and the Kleihauer-Betke test. Thalassemia and the Kleihauer-Betke test Arch Pathol Lab Med. 1982 Jan;106(1):48-9. Author …

2011年9月14日 · Measurement of the Haemoglobin F in red cell haemolysates is important in the diagnosis of δβ thalassaemia, hereditary persistence of fetal haemoglobin (HPFH) and in the …

2012年6月1日 · We report here a 33-year-old male patient who was admitted with dengue haemorrhagic fever, with a background history of Grave's disease, incidentally noted to have …

HbF levels 5% and above are more likely to be due to δβ thalassaemia or HPFH (heterocellular or pancellular). In the case of δβ thalassaemia or deletional HPFH one would expect the HbA 2 …

The first Hb analyses in Germany for the detection and identification of anomalous hemoglobin variants and thalassemia syndromes were carried out as early as 1959 in Freiburg by the …

Two of 19 transfusion-dependent patients with beta-thalassaemia have been found to have red cells indistinguishable from fetal cells on the basis of HbF content, but these patients also …

Kleihauer test negative on normal adult blood. Application: Detection and quantitation of transplacental haemorrhage. Studies in the thalassaemias. See also Flow cytometry (FMH). …

A population survey carried out in southern sardinia on more than 5000 people has shown that delta beta (F)-thalassaemia, with a gene frequency of 0-00088, is a rare trait in this population. …