Dergiler / The Ulutas Medical Journal / 2017 / Cilt: 3 - Sayı: 4

Screening for the Known Αlpha Thalassemia Deletions by Polymerase Chain Reaction

Sayfa
59–64
Yayın Tarihi
2017-10-01
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

All this ultimately provide a great help in establishing the policies for thalassemia prevention and control programs in Pakistan.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Thalassemia is the quantitatively inherited disorder of haemoglobin polypeptide chain synthesis.
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Temel Bulgular & Veri:Awareness about the exact frequency of disease in our country, Pakistan, along with the appropriate knowledge of diagnostic and prevention approach will be a step forward to combat thalassemia in Pakistan.
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Sonuç & Katkı:All this ultimately provide a great help in establishing the policies for thalassemia prevention and control programs in Pakistan.
🔬Tür:Literatür & Derleme Çalışması
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alpha Thalassemia · Deletions · Polymerase chain reaction

Abstract

Thalassemia is the quantitatively inherited disorder of haemoglobin polypeptide chain synthesis. Awareness about the exact frequency of disease in our country, Pakistan, along with the appropriate knowledge of diagnostic and prevention approach will be a step forward to combat thalassemia in Pakistan. The proposed review article will provide updated information regarding the exact frequency and distribution of thalassemia in neonates in Pakistan and Internationally. All this ultimately provide a great help in establishing the policies for thalassemia prevention and control programs in Pakistan. Thalassemia is the quantitatively inherited disorder of hemoglobin polypeptide chain synthesis. Awareness about the exact frequency of disease in our country, Pakistan, along with the appropriate knowledge of diagnostic and prevention approach will be a step forward to combat thalassemia in Pakistan. The proposed review article will provide updated information regarding the exact frequency and distribution of thalassemia in neonates in Pakistan and Internationally. All this ultimately provide a great help in establishing the policies for thalassemia prevention and control programs in Pakistan.

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Bu Makaleye Atıf Yap

BUKHARİ, K. T., NOOR, N., HUMAYOUN, S., ZAFAR, H., LAKHNANA, N. K. (2017). Screening for the Known Αlpha Thalassemia Deletions by Polymerase Chain Reaction. The Ulutas Medical Journal, Cilt: 3 - Sayı: 4, 59–64. https://ajindex.com/articles/844472

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Kaynakça (11)

  1. Stephen Raja JV, Rachchh MA, Gokani RH. Recent advances in gene therapy for thalassemia. J Pharm Bioallied Sci. 2012; 4(3):194-201.
  2. Panyasai S, Sringam P, Fucharoen G, Sanchaisuriya K, Fucharoen S. A simplified screening for α-thalassemia 1 (SEA type) using a combination of a modified osmotic fragility test and a direct PCR on whole blood cell lysates. 2002;108(2): 74-8.
  3. Neishabury M, Poorfathollah AA, Kahrizi l. Alpha thalassemia: deletion analysis in Iran.Archives Iran Med.2001; 4(4):160-4.
  4. Fucharoen S, Winichagoon P, Thonglairoam V, Siriboon W, Siritanaratkul N, Kanokpongsakdi S, et al. Prenatal diagnosis of thalassemia and hemoglobinopathies in Thailand: experience from 100 pregnancies. Southeast Asian J Trop Med Public Health. 1991;22:16-29.
  5. Pornprasert S, Wiengkum T, Srithep S, Chainoi I, Singboottra P, Wongwiwatthananukit S.Detection of α-thalassemia-1 Southeast Asian and Thai type deletions and β-thalassemia 3.5-kb deletion by single-tube multiplex real-time PCR with SYBR Green1 and high-resolution melting analysis. Korean J Lab Med. 2011 Jul;31(3):138-42.
  6. Munkongdee T, Vattanaviboon P, Thummarati P, Sewamart P, Winichagoon P, Fucharoen S, et al. Rapid diagnosis of alpha-thalassemia by melting curve analysis. J Mol Diagn. 2010;12:354-358.
  7. Gapor SA, Bakar AMZ, Farouk AFA. Explaining ethnic relations in Malaysia through the “concentric circle model”: case studies of the states of Perak and Kelantan, Malaysia. European Journal of Social Sciences. 2009;12(2):252-258.
  8. Sriroongrueng W, Pornpatkul M, Panich V, Fucharoen S. α- thalassemia incidence in southern Thailand by restriction endonuclease analysis of globin DNA from placental blood at Songklanagarind hospital. Southeast Asian Journal of Tropical Medicine and Public Health. 1997;28(supplement 3):93–96
  9. Zygulska LM, Eigel A, Helbig B, Sanguansermsri T, Horst J, Flatz G. Prevalence of α-thalassemias in northern Thailand. Human Genetics. 1996;98(3):345–347.
  10. Rosnah B, Rosline H, Ain FA. Detection of Common Deletional Alpha-Thalassemia Spectrum by Molecular Technique in Kelantan, Northeastern Malaysia. ISRN Haematol. 2012;46(2):989. Mohan H. The haematopoietic system. In: Mohan H, Mohan P, Mohan T, editors. The textbook of pathology. 5th ed. New Delhi: Jaypee Brothers Medical Publishers; 2008. pp. 397– 402. Mouélé R, Pambou O, Feingold J, Galactéros F. α- thalassemia in Bantu population from Congo-Brazzaville: its interaction with sickle cell anemia. Human Heredity. 2000;50(2):118–125.
  11. Burgess-Beusse B, F