Literature DB >> 416639

Different types of beta-thalassemia intermedia. A genetic study in 20 patients.

M Aksoy, G Dinçol, S Erdem.   

Abstract

20 patients with beta-thalassemia intermedia classified according to the results of genetic studies are presented. (1) 9 patients with beta-thalassemia intermedia homozygous for beta-thalassemia with increased Hb-A2 are reported. (2) 8 patients with beta-thalassemia intermedia, 3 homozygous for beta-thalassemia with normal levels of Hbs.A2 and F, 5 heterozygous for both this and beta-thalassemia with increased Hb-A2 are presented. (3) 2 families with beta-thalassemia intermedia heterozygous for both beta-thalassemia with increased HbA2 and 'silent" beta-thalassemia are reported. Two different varieties are presented.

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Year:  1978        PMID: 416639     DOI: 10.1159/000207760

Source DB:  PubMed          Journal:  Acta Haematol        ISSN: 0001-5792            Impact factor:   2.195


  6 in total

1.  The molecular basis of beta-thalassemia in Turkey.

Authors:  A N Başak; H Ozçelik; A Ozer; A Tolun; M Aksoy; L Ağaoğlu; F Ridolfi; L Ulukutlu; N Akar; A Gürgey
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

2.  Clinical heterogeneity of silent-gene b-thalassemia among Indians.

Authors:  A Nadkarni; A Pawar; V C Mudera; D Mohanty; R Colah
Journal:  Ann Hematol       Date:  1995-01       Impact factor: 3.673

3.  A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia.

Authors:  R Galanello; L Maccioni; M C Rosatelli; P Ibba; A M Nurchi; A Cao
Journal:  J Med Genet       Date:  1984-04       Impact factor: 6.318

4.  beta+-Thalassemia intermedia with low HbF.

Authors:  M A Zago; F F Costa; C Bottura
Journal:  Klin Wochenschr       Date:  1983-01-17

5.  Thalassaemia intermedia in a family with beta 0-thalassaemia and Hb Hasharon.

Authors:  M A Zago; F F Costa; C Bottura
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

6.  Heterogeneity in beta 0 thalassemia from Algeria: genetic, clinical and molecular studies.

Authors:  M Belhani; F Morlé; P Colonna; J Godet
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

  6 in total

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