Immunologic Diagnosis of α-Thalassemia Traits
- 1 January 1979
- journal article
- research article
- Published by Taylor & Francis in Hemoglobin
- Vol. 3 (1) , 21-31
- https://doi.org/10.3109/03630267909069152
Abstract
Frequently it is impossible to diagnose .alpha.-thalassemia-2 trait from hematologic findings, since the red cell morphology and the MCV [mean corpuscular volume] are normal. In such cases, after the neonatal period Hb Bart''s is not detectable by conventional electrophoreses and chromatography. Antibody against Hb Bart''s was produced in rabbits by repeated injections with Hb Bart''s from Hb Bart''s hydropic fetuses. The antibody was specific for Hb Bart''s without cross-reaction with Hbs A, A2, E, F and H. By the capillary tube precipitin test Hb Bart''s was demonstrable in 82% of 87 obligatory cases for .alpha.-thalassemia traits, 86% in .alpha.-thalassemia-1 trait and 79% in .alpha.-thalassemia-2 trait. The test was positive in 21% of the general subjects, corresponding to the prevalence of .alpha.-thalassemia in Bangkok. The immunologic demonstration of Hb Bart''s appears to offer a diagnostic screening test for .alpha.-thalassemia traits in the postneonatal period.This publication has 7 references indexed in Scilit:
- Identification of a Nondeletion Defect in α-ThalassemiaNew England Journal of Medicine, 1977
- α-THALASSAEMIA IN THE UNITED KINGDOMBritish Journal of Haematology, 1977
- Deletion of α-globin genes in haemoglobin-H disease demonstrates multiple α-globin structural lociNature, 1975
- Haemoglobin Bart's in Saudi ArabiaBritish Journal of Haematology, 1975
- DIFFERENTIATION OF IRON DEFICIENCY FROM THALASSÆMIA TRAIT BY ROUTINE BLOOD-COUNTThe Lancet, 1973
- Studies on haemoglobin Bart's (Hb??4) in Thailand: the incidence and the mechanism of occurrence in cord blood*Annals of Human Genetics, 1967
- Hæmoglobin H Disease in Thailand: a Genetical StudyNature, 1964