Dergiler / Turkish Journal of Medical Sciences / 2017 / Cilt: 47 - Sayı: 3

Development of a new real-time PCR screening kit for HbS and common beta-thalassemia mutations observed in Turkey

Sayfa
973–978
Yayın Tarihi
2017-06-01
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Conclusion: This reliable kit provided rapid diagnosis including 76% of the β-thalassemia mutations in Turkey.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Background/aim: IVSI-110 (G>A), IVSI-6 (T>C), IVSII-1 (G>A), IVSII-745 (C>G), IVSI-1 (G>A), and HbS are mutations covering 76% of all the β-globin mutations in the Turkish population.
📊
Temel Bulgular & Veri:Materials and methods: This study included 100 individuals with beta-thalassemia or sickle cell anemia who had unknown mutations, and 21 controls with known mutations.
💡
Sonuç & Katkı:Conclusion: This reliable kit provided rapid diagnosis including 76% of the β-thalassemia mutations in Turkey.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Beta-thalassemia · HbS · β-thalassemia screening kit

Abstract

Background/aim: IVSI-110 (G>A), IVSI-6 (T>C), IVSII-1 (G>A), IVSII-745 (C>G), IVSI-1 (G>A), and HbS are mutations covering 76% of all the β-globin mutations in the Turkish population. In this study, our aim is to develop a reliable, fast, real-time kit for these mutations using the TaqMan probe method. Materials and methods: This study included 100 individuals with beta-thalassemia or sickle cell anemia who had unknown mutations, and 21 controls with known mutations. Results: We designed a kit containing the IVSI-110 (G>A), IVSI-6 (T>C), IVSII-1 (G>A), IVSII-745 (C>G), IVSI-1 (G>A), and HbS mutations by using the real-time PCR method. One hundred patients were studied with our developed TaqMan real-time PCR kit. Of these patients, 73 (73%) were identified with the beta gene mutation. Among those 73 patients, 16 were homozygous, 54 were heterozygous, and 3 were compound heterozygous. Conclusion: This reliable kit provided rapid diagnosis including 76% of the β-thalassemia mutations in Turkey.

🔖

Bu Makaleye Atıf Yap

KARAER, D. K., ERGÜN, M. A., RUHİ, H. İ., ÖZTÜRK, J., KARA, H., ÇAKMAK, D. R., AYDOĞMUŞ, T., PERÇİN, F. E. (2017). Development of a new real-time PCR screening kit for HbS and common beta-thalassemia mutations observed in Turkey. Turkish Journal of Medical Sciences, Cilt: 47 - Sayı: 3, 973–978. https://ajindex.com/articles/112684

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...