Term Paper on "Recent Advances Within the Last 10 Years in the Treatment of Muscular Dystrophy"
Term Paper 4 pages (1456 words) Sources: 10
[EXCERPT] . . . .
Advances in Muscular DystrophyMuscular Dystrophy
Muscular dystrophy (MD) is a genetic disorder that results in progressive muscular degeneration particularly those of the skeletal system (Dalkilic and Kunkel, 2003). MD impacts both skeletal and cardiac muscles which can result in progressive loss of ambulation as well as respiratory and cardiac functioning (Trollet et al., 2009). Today there are over thirty genes that are known to contribute to the various forms of musclular dystrophy which result in symptoms of varying degrees. The most common form of MD is Duchenne MD which is caused by a mutation in the dystrophin gene and impacts 1 in 3500 males born (Trollet et al., 2009). There are also several other forms of MD including limb-girdle congenital, facioscapulohumeral, myotonic, oculopharyngeal, distal and Emery -- Dreifuss muscular dystrophy (Trollet et al., 2009). Each type of MD has been categorized by clinical presentation, method of inheritance, age of onset, and progression of illness (Lovering et al., 2005). Research into the field of MD regularly uncovers new genes that contribute to the manifestation of this illness as well as providing insight into the complexity of this illness.
In order for any treatment to impact the progression of the illness or better yet cure the disease, we must have a thorough understanding of the pathogenesis of the disorder (Mhashilkar et al., 2001). Although the pathogenesis of MD is fairly well understood the ability to provide adequate treatment is confounded by the fact that the skeletal muscle is the largest body tissue, comprising 30% of the total body mass and is widely distributed (Clemens and Duncan, 200
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While there are no present corrective therapies for MD many of the current therapies geared at supportive and preventative care include surgery, corticosteroid administration for muscle weakness, cardiovascular medication to treat cardiomyopathy, ventilation for respiratory issues, and physiotherapy (Trollet et al., 2009). While these treatments focus on the disease progression and attempt to alleviate symptoms, they are unable to address the pathogenesis of the disease itself. However, recent advances in genetics, molecular biology and muscle physiology have resulted in new strategies to treat the disease phenotype. The most common treatments include gene therapy, cell replacement therapy, psychopharmacological approaches, exon, as well
Gene therapy has been aimed at mitigating the genetic deficiencies that have led to symptoms in patients with MD. Trollet et al. (2009) describe gene therapy as the introduction of a therapeutic nucleic acid into targeted cells in order to alter the physiology of the cells. Gene therapies have emphasized the restoration of a functional dystrophin gene through the use of whole cells, plasmid and viral vectors, gene correction strategies, and upregulation of homologous genes (McClorey et al., 2005). One of the major challenges in the development of gene therapy for muscular dystrophy includes the need to target specific muscles for each manifestation of MD (Trollet et al., 2009). This can be challenging since muscle tissue makes up such a significant portion of total body mass.
Despite the significant potential that gene therapy has for patients with MD, it still remains in the preclinical and clinical trial stages of intervention. Still one should be cautiously optimistic about the potential of full implementation of gene therapy in MD patients while being mindful of the many hurdles that researchers face when translating successes with animals to human subjects. In order to achieve successful gene therapy to muscle will require a regional or systemic intravascular route of delivery to efficiently transducer skeletal muscle (Clemens and Duncan, 2001). There are concerns about the manner in which the body's immune defense mechanisms will react to the gene transfer and whether or not the innate responses will lead the body to attack the transplanted cells. These concerns have only been found in high doses… READ MORE
Quoted Instructions for "Recent Advances Within the Last 10 Years in the Treatment of Muscular Dystrophy" Assignment:
The title given is Recent advances (within the last 10 years) in the treatment of muscular dystrophy.
Please try to compare the 10 recent that are listed in ADVANCES IN DUCHENNE MUSCULAR DYSTROPHY GENE THERAPY nature oct 2003.
But I would prefer if that you could specify the most ideal way(s) to proceed with mitigating muscular dystrophy in general, not just duchenne.
This essay for my intro biology class has a limit of 1300 words.
There are also other references that i will provide but i am so confounded by what they r saying.
This term paper should be a critical analysis on all the recent advances.
I would think that elaborating on what muscular dystrophy is is not important and probably just used for the intro. probably inclusion of diagrams shld be appropriate as well.
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How to Reference "Recent Advances Within the Last 10 Years in the Treatment of Muscular Dystrophy" Term Paper in a Bibliography
“Recent Advances Within the Last 10 Years in the Treatment of Muscular Dystrophy.” A1-TermPaper.com, 2010, https://www.a1-termpaper.com/topics/essay/advances-muscular-dystrophy/38397. Accessed 29 Jun 2024.
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