Literature DB >> 638060

Variations in globin synthesis in delta-beta-thalassaemia.

T R Kinney, S Friedman, E Cifuentes, H C Kim, E Schwartz.   

Abstract

Peripheral blood globin synthesis studies were done in 11 patients with delta beta-thalassaemia trait, Hb S-delta beta-thalassaemia or delta beta/betao-thalassaemia from two black and two Caucasian families. All patients had elevated Hb F and normal or decreased Hb A2 levels and 10 had family studies confirming the diagnosis. In addition, four unrelated non-thalassaemic patients with elevated Hb F levels also had peripheral blood globin synthesis studies. The beta/alpha specific activity globin synthesis ratios in the three blacks with delta beta-thalassaemia trait were 0.60--1.04. In the four Caucasians with delta beta-thalassaemia traint, the beta/alpha ratios were 0.58--1.02. These results demonstrate a wide range of ratios overlapping those of normal controls (0.99 +/- 0.06). The betas/alpha ratios in three blacks with Hb S-delta beta-thalassaemia ranged from 0.66 to 1.00, similar to those of patients with delta beta-thalassaemia trait. In the black patient with delta beta/betao-thalassaemia, the gamma/alpha ratio was 0.67. The beta/alpha peripheral blood ratios in the four non-thalassaemia patients with elevated Hb F ranged from 1.00 to 1.11, similar to those of normal controls. These studies indicate that a decreased beta/alpha ratio is not an invariable finding in delta beta-thalassaemia in blacks or Caucasian patients and that globin synthesis data alone is insufficient to diagnose definitively heterozygotes for delta beta-thalassaemia or to distinguish this trait from non-thalassaemic haematological disorders associated with a normal percentage of Hb A2 and an elevated level of Hb F.

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Year:  1978        PMID: 638060     DOI: 10.1111/j.1365-2141.1978.tb07103.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  4 in total

1.  Interaction of alpha- and delta beta o- thalassaemia: haematological features and globin chain synthesis analysis.

Authors:  R Galanello; M Furbetta; M A Melis; C Rosatelli; A Cao
Journal:  J Med Genet       Date:  1981-02       Impact factor: 6.318

2.  G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C.

Authors:  D R Higgs; J B Clegg; W G Wood; D J Weatherall
Journal:  J Med Genet       Date:  1979-08       Impact factor: 6.318

3.  Delta beta (F)-thalassaemia in Sardinia.

Authors:  A Cao; M A Melis; R Galanello; A Angius; M Furbetta; P Giordano; L F Bernini
Journal:  J Med Genet       Date:  1982-06       Impact factor: 6.318

4.  Homozygous delta-beta Thalassemia in a Child: a Rare Cause of Elevated Fetal Hemoglobin.

Authors:  S Verma; M Bhargava; Sk Mittal; R Gupta
Journal:  Iran J Ped Hematol Oncol       Date:  2013-01-22
  4 in total

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