Journals / Turkish Journal of Hematology / 2001 / Cilt: 18 - Sayı: 4

Beta-thalassemia mutations in the East of Turkey

Pages
239–242
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

We conclude that although five different 6-thalassemia mutation exist in Van Lake region, 6-thalassemia is not a potential risk in the east of Turkey.

📌 3 Key Takeaways

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Objective & Hypothesis:This study was planned to determine the frequency of 6-thalassemia trait and mutations in Van Lake region, which is in the eastern part of Turkey, surrounded by Iran in the east and by lraq in the south.
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Key Findings & Data:This study consist of 1014 healthy students, between the age of 12 and 18 years who are studying in boarding schools in Van city and cities surrounding Van Lake that includes Van, Ağrı, Hakkari, Bitlis, Muş and Siirt.
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Conclusion & Impact:We conclude that although five different 6-thalassemia mutation exist in Van Lake region, 6-thalassemia is not a potential risk in the east of Turkey.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Ergenlik · Yaygınlık · Eritrosit indeksleri

Özet

This study was planned to determine the frequency of 6-thalassemia trait and mutations in Van Lake region, which is in the eastern part of Turkey, surrounded by Iran in the east and by lraq in the south. This study consist of 1014 healthy students, between the age of 12 and 18 years who are studying in boarding schools in Van city and cities surrounding Van Lake that includes Van, Ağrı, Hakkari, Bitlis, Muş and Siirt. The students were randomly selected according to their school numbers. Their origin was not taken into consideration in selection. Complete blood counts were performed on all donors. The accepted lower limit of mean corpuscular volume (MCV) and mean corpuscular hemoglobin (MCH) were 78 fL and 27 pg respectively. HbAg was measured by DE-52 microcolumn chromatography method. 6-thalassemia trait with high HbAj was found in 6 children. 6-thalassemia homozygous form of -30 (T-A) mutation was determined in one child and HbD-Los An-geles heterozygous in another. The 6-thalassemia homozygous individual was accepted as two cases in prevalence calculation. We found that the prevalence of 6-thalassemia trait was 0.78% in this area. in DNA analyses, there were 6-thalassemia gene mutations of FSC 8/9 (+G), -30 (T-A), IVS1-110 (G-A), IVS ll-l (G-A) and IVS 1-130 (G-A) in 3, 2, l, l and l individuals, respectively. We conclude that although five different 6-thalassemia mutation exist in Van Lake region, 6-thalassemia is not a potential risk in the east of Turkey.

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Cite This Article

ÖNER, A. F., ÖZER, R., ÜNER, A., ARSLAN, Ş., GÜMRÜK, F. (2001). Beta-thalassemia mutations in the East of Turkey. Turkish Journal of Hematology, Cilt: 18 - Sayı: 4, 239–242. https://ajindex.com/articles/412981

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