Genotype-phenotype analysis in HbS-beta-thalassemia

被引:8
作者
Altay, C
Oner, C
Oner, R
Mesci, L
Balkan, H
Tuzmen, S
Basak, AN
Gumruk, F
Gurgey, A
机构
[1] HACETTEPE UNIV,SCH MED,DEPT PEDIAT,ANKARA,TURKEY
[2] HACETTEPE UNIV,SCH MED,DEPT BIOL,ANKARA,TURKEY
[3] BOGAZICI UNIV,SCH ARTS & SCI,DEPT GENET & MOL BIOL,ISTANBUL,TURKEY
关键词
sickle cell; beta-thalassemia mutations; sickle cell beta-thalassemia;
D O I
10.1159/000154404
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genotypes and phenotypes were studied in 31 Turkish HbS-beta-thalassemia patients. In 19 patients the beta-thalassemia mutations were beta(+) and in 12 the beta(0) phenotype. The IVSI-110 mutation was found in 45% of the patients. IVSI-1, beta 39, IVSII-1 and FSC8 are the genotypes associated with beta(0)-thalassemia. Hematological data were evaluated at the time of diagnosis and 4 years after diagnosis. The mean HbF value was 13 +/- 7.8% at diagnosis and 9.7 +/- 7.8% 4 years later. A significant negative correlation was observed between the age of the patients and the HbF value (p < 0.05). No statistically significant differences were observed between the mean of hematological parameters in beta(+)- and beta(0)-thalassemia patients except for the mean HbF value which were 10.7 +/- 6.9 and 15.9 +/- 7.7% in beta(+)- and beta(0)-thalassemia, respectively (p < 0.05), The study indicated that beta-thalassemia mutations in trans to the HbS mutation do not exert any beneficial effect on the manifestation of the disease.
引用
收藏
页码:161 / 164
页数:4
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