An overview of Diagnostic Approaches for Detection of Duchunne Muscular Dystrophy (DMD)/Becker Muscular Dystrophy (BMD)

Gaurava Srivastava and Preeti Srivastava
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Preeti Srivastava: Genetic Centre, Government Medical College and Hospital, India

Current Trends in Biomedical Engineering & Biosciences, 2017, vol. 8, issue 2, 36-43

Abstract: D/BMD is an X-linked recessive disorder characterized by progressive muscle weakness, which predominantly affect males. This study intended to elucidate overview of available diagnostic approaches utilized for detection of D/BMD. Till date no absolute cure of the disease is available to be used in clinical practice. Early diagnosis and timely management are requisite for D/BMD and it enhances the quality of life of patients. Various diagnostic approaches for D/BMD includes Clinical features, biochemical analysis, molecular analysis, muscle biopsy, electrodiagnostic approach, imaging tests, NCV, Pedigree and family history, IQ measurement, genetic counseling of families for carrier detection and prenatal screening.

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Date: 2017
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Persistent link: https://EconPapers.repec.org/RePEc:adp:jctbeb:v:8:y:2017:i:2:p:36-43

DOI: 10.19080/CTBEB.2017.08.555733

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