Thalassaemia of intermediate severity resulting from the interaction between alpha- and beta-thalassaemia.
Open Access
- 1 December 1978
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 15 (6) , 448-451
- https://doi.org/10.1136/jmg.15.6.448
Abstract
A Sicilian family is described in which the alpha-thalassaemia gene is interacting in several members with beta-thalassaemia resulting in a balanced alpha/beta chain production ratio. In one patient, affected by homozygous beta-thalassaemia, the presence of alpha-thalassaemia resulted in a less severe clinical expression of the disease, less marked imbalance in the alpha/non-alpha ratio, and a lower level of HbF. Further studies of haemoglobin synthesis are needed to clarify the complex genetic picture that results from the interaction of different forms of thalassaemia.This publication has 9 references indexed in Scilit:
- The Clinical and Biosynthetic Characterization of αβ-ThalassaemiaBritish Journal of Haematology, 1972
- α-Thalassemia in the American NegroJournal of Clinical Investigation, 1972
- Mild thalassemia: the result of interactions of alpha and beta thalassemia genesJournal of Clinical Investigation, 1970
- ALPHA‐ AND BETA‐THALASSEMIA IN THAILAND*Annals of the New York Academy of Sciences, 1969
- Excess α Chain Synthesis Relative to β Chain Synthesis in Thalassaemia Major and MinorNature, 1966
- Abnormal human haemoglobins: Separation and characterization of the α and β chains by chromatography, and the determination of two new variants, Hb chesapeake and Hb J (Bangkok)Journal of Molecular Biology, 1966
- Alpha-Beta Thalassemia Disease in a Negro FamilyNew England Journal of Medicine, 1966
- A Possible Case of Alpha-Beta ThalassaemiaHuman Heredity, 1962
- THE OSMOTIC RESISTANCE (FRAGILITY) OF HUMAN RED CELLS 1Journal of Clinical Investigation, 1947