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Gunn Abilities United Club
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Muscular Dystrophy February 2014
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Muscular Dystrophy Muscular dystrophy (MD) – group of diseases that weaken the skeletal system, affecting movement and mobility Defects in muscle proteins, death of muscle cells and tissues Discovered in 1860s – Guillame Duchenne observed thirteen boys who lost the ability to walk, eventually dying at a young age The most common type of muscular dystrophy – Duchenne muscular dystrophy – is named after him!
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How does muscular dystrophy affect people? Thanks to Patient.co.uk
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Symptoms Muscle weakness – even as early as age three! Begins in hip/pelvic area and migrates toward arms and legs “Muscles” doesn’t just mean voluntary muscles (like the muscles in your arm) – it can also include respiratory muscles! Until very recently, life expectancy for people with muscular dystrophy was extremely low, usually up to early teenage years!
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Research and Possible Hope Scientists are currently developing key technologies toward solving muscular dystrophy and many other genetic diseases We’ll discuss two: gene therapy and exon skipping
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Option 1: Gene Therapy Gene therapy – delivery or replacement of genes as a way of treating a disease Produce different proteins that directly or indirectly affect a person’s symptoms Why difficult? Genes have to targeted and delivered in appropriate areas; we can’t have the immune system targeting the vehicles carrying the genes!
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Option 2: Exon Skipping Recall that the genetic code is dependent on the order of base pairs Cells read these base pairs in units of three nucleotides (ex: ATC or TCG) – if the order is shifted, the “reading frame” is skewed Scientists currently are trying to “skip” some of the nucleotides that create a dysfunctional protein – hence the name exon skipping Unfortunately, many regulations exist for exon skipping
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Option 2: Exon Skipping (cont.) Scientists use an alternate oligonucleotide to skip a section of DNA that codes for a dysfunctional protein Thanks to Skeletal Muscle Journal
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Curious? Learn more from the Muscular Dystrophy Association! Google! Ask about muscular dystrophy to one of the officers!
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What’s the cause? Generally genetically inherited (follows inheritance patterns) Located on X chromosome; males more likely to be affected Recent research has shown that mutations of the protein dystrophin are possible in ~33% of people affected by Duchenne muscular dystrophy Dystrophin – protein that helps connect the cytoskeleton of a muscle fiber to its surroundings Bottom line – lack of dystrophin = muscle degeneration Thanks to Sanger Institute
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What can I do to help? Join the Muscular Dystrophy Association – a movement and association dedicated toward helping those with muscular dystrophy MDA clinic in Lucile Packard Hospital – Lucile Packard Children’s Hospital Pediatrics Neuromuscular Clinic! Many patients with muscular dystrophy are also patients at the VA in Palo Alto! Contact Alex Wong (alx.wong1997@gmail.com) for more information regarding volunteer opportunities Begin your own movement!
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Thank You
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