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The Spectrum of β-Thalassemia Mutations in Batman, South-Eastern Turkey

Yıl 2020, Cilt: 47 Sayı: 4, 828 - 835, 30.12.2020
https://doi.org/10.5798/dicletip.850314

Öz

Kaynakça

  • 1. Clarke GM, Higgins TN. Laboratory Investigation of Hemoglobinopathies and Thalassemias: Review and Update. Clin Chem 2000; 46: 1284-90.

The Spectrum of β-Thalassemia Mutations in Batman, South-Eastern Turkey

Yıl 2020, Cilt: 47 Sayı: 4, 828 - 835, 30.12.2020
https://doi.org/10.5798/dicletip.850314

Öz

Objective: In this study, we aimed to determine the mutation types and the frequencies of these mutations in the patients with thalassemia in Batman province and to provide the use of these findings in genetic counselling.
Methods: The study included 46 patients (27 male and 19 female) with a mean age of 9.5 ± 3.6 years (range: 3-16 years). In this study, mutations were determined by sequence analysis method.
Results: 7 different mutations were detected in patients. IVS-I-110 (G>A) (56.25%), codon 44 (-C) del (16.25%), IVS-I-1 (G>A) (12.5%), IVS- II-1 (G>A) (6.25%) were the most common and they were found to constitute 91.25% of the cases. As in other regions of Turkey, IVI-1-110 (G >A) was the most frequent mutation detected. In this study; 28 mutant alleles including IVS-I-110 (G>A)/IVS-I-1 (G> A) (4), IVS-I-110 (G>A)/IVS-II-1 (G> A) (4), codon 8 (-AA) del/IVS-1-110 (G>A) (1), codon 8 (-AA) del/ codon 44 (-C)del (1), codon 15 (GG-GA)/codon 44 (-C) del (1), codon 44 (-C) del/IVS-I-1 (G> A) (1), codon 44 (-C) del/ IVS-II-1 (G> A) (1), codon 44 (-C)del/IVS-I-110 (G>A) (1) were found to have formed a compound heterozygous mutation. Among the β-thalassemia patients in Batman province, 29 (56.25%) were determined to have β⁺ mutation, and 26 (43.75%) had β° mutation.
Conclusion: It is important that we, in our study, discovered IVS-II-1 (G>A) mutation compounded with heterozygous in five patients and codon 8 (-AA) del mutation as homozygous in one patient who presented a clinical manifestation of thalassemia intermedia despite having homozygous beta thalassemia. These results will contribute to genetic counseling and prenatal diagnosis.

Kaynakça

  • 1. Clarke GM, Higgins TN. Laboratory Investigation of Hemoglobinopathies and Thalassemias: Review and Update. Clin Chem 2000; 46: 1284-90.
Toplam 1 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Sağlık Kurumları Yönetimi
Bölüm Original Articles
Yazarlar

Sedat Yilmaz Bu kişi benim

Yayımlanma Tarihi 30 Aralık 2020
Gönderilme Tarihi 17 Nisan 2020
Yayımlandığı Sayı Yıl 2020 Cilt: 47 Sayı: 4

Kaynak Göster

APA Yilmaz, S. (2020). The Spectrum of β-Thalassemia Mutations in Batman, South-Eastern Turkey. Dicle Tıp Dergisi, 47(4), 828-835. https://doi.org/10.5798/dicletip.850314
AMA Yilmaz S. The Spectrum of β-Thalassemia Mutations in Batman, South-Eastern Turkey. diclemedj. Aralık 2020;47(4):828-835. doi:10.5798/dicletip.850314
Chicago Yilmaz, Sedat. “The Spectrum of β-Thalassemia Mutations in Batman, South-Eastern Turkey”. Dicle Tıp Dergisi 47, sy. 4 (Aralık 2020): 828-35. https://doi.org/10.5798/dicletip.850314.
EndNote Yilmaz S (01 Aralık 2020) The Spectrum of β-Thalassemia Mutations in Batman, South-Eastern Turkey. Dicle Tıp Dergisi 47 4 828–835.
IEEE S. Yilmaz, “The Spectrum of β-Thalassemia Mutations in Batman, South-Eastern Turkey”, diclemedj, c. 47, sy. 4, ss. 828–835, 2020, doi: 10.5798/dicletip.850314.
ISNAD Yilmaz, Sedat. “The Spectrum of β-Thalassemia Mutations in Batman, South-Eastern Turkey”. Dicle Tıp Dergisi 47/4 (Aralık 2020), 828-835. https://doi.org/10.5798/dicletip.850314.
JAMA Yilmaz S. The Spectrum of β-Thalassemia Mutations in Batman, South-Eastern Turkey. diclemedj. 2020;47:828–835.
MLA Yilmaz, Sedat. “The Spectrum of β-Thalassemia Mutations in Batman, South-Eastern Turkey”. Dicle Tıp Dergisi, c. 47, sy. 4, 2020, ss. 828-35, doi:10.5798/dicletip.850314.
Vancouver Yilmaz S. The Spectrum of β-Thalassemia Mutations in Batman, South-Eastern Turkey. diclemedj. 2020;47(4):828-35.