Literature DB >> 23613656

Detection of β-globin Gene Mutations Among β-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction.

Syahzuwan Hassan1, Rahimah Ahmad, Zubaidah Zakaria, Zefarina Zulkafli, Wan Zaidah Abdullah.   

Abstract

BACKGROUND: β-thalassaemia is one of the most common single-gene disorders worldwide. Each ethnic population has its own common mutations, accounting for the majority of cases, with a small number of mutations for the rarer alleles. Due to the heterogeneity of β-thalassaemia and the multi-ethnicity of Malaysians, molecular diagnostics may be expensive and time consuming.
METHODS: A simple polymerase chain reaction (PCR) approach involving a multiplex amplification refractory mutation system (MARMS) and one amplification refractory mutation system (ARMS), consisting of 20 β-globin gene mutations, were designed and employed to investigate β-thalassaemia patients and carriers.
RESULTS: Out of 169 carriers tested with the MARMS, Cd 41/42 (-TTCT), Cd 26 (A-G) HbE, IVS 1-1 (G-T), and IVS 1-5 (G-C) were the most common mutations, accounting for 78.1%. Among the Malays, Cd 26 (A-G) HbE, Cd 41/42 (-TTCT), IVS 1-1 (G-T), and IVS 1-5 (G-C) were the most common mutations, accounting for 81.4%, whereas Cd 41/42 (-TTCT) and IVS 2-654 (C-T) were most common among the Chinese (79.1%).
CONCLUSION: We propose the use of this cheap, easy to interpret, and simple system for the molecular diagnostics of β-thalassaemia among Malaysians at the Institute for Medical Research (IMR).

Entities:  

Keywords:  MARMS; Molecular diagnostics; β-globin gene mutations; β-thalassaemia

Year:  2013        PMID: 23613656      PMCID: PMC3629881     

Source DB:  PubMed          Journal:  Malays J Med Sci        ISSN: 1394-195X


  22 in total

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Review 10.  Molecular diagnosis of haemoglobin disorders.

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5.  Mutation analysis of β-thalassemia in East-Western Indian population: a recent molecular approach.

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7.  Co-existence of myeloproliferative neoplasias and β-thalassemia with IVS-2-654 mutation-a case report.

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