Muscular Dystrophy essays

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3 Pages 1555 Words
Muscular dystrophy is a genetic disease that currently has no cure. There are medical treatments and medications that can help ease symptoms and manage the disease. We will discuss further later what these treatments and medications are and how they can help the patient. Let's first briefly discuss the history of muscular dystrophy and how the disease propagates. Muscular dystrophy...
3 Pages 1262 Words
The developmental condition that I thought would be the most beneficial to learn to enhance my chiropractic career is muscular dystrophy. Muscular dystrophy is categorized as rare genetic diseases, that displays numerous symptoms, however, the main apparent symptom is loss of muscle function (Do et al. 2018). The abnormality that appears with muscular dystrophy is that abnormal genes interrupt the...
6 Pages 2779 Words
Introduction: Muscular dystrophies are defined as a group of heterogeneous group of diseases characterized by muscle weakness (Rahimov et al, 2013). There are different kinds of muscular dystrophy like Duchenne, Becker, Myotonic, Congenital, Emery-Dreifuss, Facioscapulohumeral, Limb-girdle, Distal, and Oculopharyngeal (Table 1). The most common form is Duchenne muscular dystrophy (DMD). 1 in every 3500 to 5000 newborn males worldwide are...
3 Pages 1231 Words
Duchenne’s Muscular Dystrophy is a genetic disorder linked to the X chromosome that is caused by a deficiency in the protein dystrophin (Mendell et al., 1995). This disease weakens skeletal and cardiac muscles, and may pose obstacles when sitting, standing, walking, and speaking. Treatment by myoblast transfer showed promising results in animal trials. This method strives to replace dystrophin through...
3 Pages 1553 Words
Introduction: An ongoing investigation has indicated that CRISPR can be utilized as a generative method that can treat Duchenne muscular dystrophy. Because of an examination in mice, it could be created as a remedial choice for humans Duchenne muscular dystrophy is caused by a defective gene for dystrophin. Duchenne muscular dystrophy occurs in about 1 out of every 3,600 males...
5 Pages 2385 Words
Inquiry Question: Should funding be allocated towards further research into genome editing as a clinical treatment for Duchenne Muscular Dystrophy? Introduction: Duchenne Muscular Dystrophy is a form of inherited neuromuscular disease found in children, causing progressive degeneration of muscle stability. It is as a result of a mutation in the DMD gene coding for the protein called dystrophin. A mutation...
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