2008•Journal of Brain and Nervous DiseasesRequires access

Detection of Duchenne/Becker muscular dystrophy gene deletions with multiplex-PCR

WU Bao-ren

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Abstract

Objective:To analyses the deletion distribution of Dystrophin gene in Duchenne/Becker muscular dystrophy(DMD/BMD) patients.To analyses the experimental method.Methods:Forty patients with DMD/BMD and five healthy people were screened with multiplex-PCR(mPCR) using eighteen pairs of primers.Results:Different exon deletions were detected in twenty-seven cases(67.5%),thirteen cases(32.5%) were not.The deletions of sixteen cases were located in exons 44-52,six in exons 2-20 and five in the both,especially in exon 45,48 and 51.Conclusion:Gene deletion is mainly distributed in two hot spot around exons 44-52 and 2-20.Multiplex-PCR is a valuable method in clinical diagnosis.

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Objective:To analyses the deletion distribution of Dystrophin gene in Duchenne/Becker muscular dystrophy(DMD/BMD) patients.To analyses the experimental method.Methods:Forty patients with DMD/BMD and five healthy people were screened with multiplex-PCR(mPCR) using eighteen pairs of primers.Results:Different exon deletions were detected in twenty-seven cases(67.5%),thirteen cases(32.5%) were not.The deletions of sixteen cases were located in exons 44-52,six in exons 2-20 and five in the both,especially in exon 45,48 and 51.Conclusion:Gene deletion is mainly distributed in two hot spot around exons 44-52 and 2-20.Multiplex-PCR is a valuable method in clinical diagnosis.

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Available abstract

Objective:To analyses the deletion distribution of Dystrophin gene in Duchenne/Becker muscular dystrophy(DMD/BMD) patients.To analyses the experimental method.Methods:Forty patients with DMD/BMD and five healthy people were screened with multiplex-PCR(mPCR) using eighteen pairs of primers.Results:Different exon deletions were detected in twenty-seven cases(67.5%),thirteen cases(32.5%) were not.The deletions of sixteen cases were located in exons 44-52,six in exons 2-20 and five in the both,especially in exon 45,48 and 51.Conclusion:Gene deletion is mainly distributed in two hot spot around exons 44-52 and 2-20.Multiplex-PCR is a valuable method in clinical diagnosis.

Key concepts: Exon, Multiplex polymerase chain reaction, Duchenne muscular dystrophy, Muscular dystrophy, Genetics, Gene, Multiplex, Biology

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