Different Types of Beta-Thalassemia Intermedia
- 1 January 1978
- journal article
- research article
- Published by S. Karger AG in Acta Haematologica
- Vol. 59 (3) , 178-189
- https://doi.org/10.1159/000207760
Abstract
20 patients with β-thalassemia intermedia classified according to the results of genetic studies are presented. (1) 9 patients with β-thalassemia intermedia homozygous for β-thalassemia with increased Hb-A2 are reported. (2) 8 patients with β-thalassemia intermedia, 3 homozygous for β-thalassemia with normal levels of Hbs.A2 and F, 5 heterozygous for both this and β-thalassemia with increased Hb-A2 are presented. (3) 2 families with β-thalassemia intermedia heterozygous for both β-thalassernia with increased Hb-A2 and ‘silent’ β-thalassemia are reported. Two different varieties are presented.Keywords
This publication has 4 references indexed in Scilit:
- EFFECT OF IRON DEFICIENCY ON LEVELS OF HEMOGLOBINS A2 AND E1968
- Mild Homozygous Beta-ThalassemiaAnnals of Internal Medicine, 1966
- THALASSAEMIA SYNDROMES - GENETIC STUDIES ON THALASSAEMIA MINOR WITH LARGE AMOUNTS OF FETAL HAEMOGLOBIN1965
- The Thalassaemia SyndromesActa Haematologica, 1961