Muscular dystrophies (MDs) are a group of genetic diseases with progressive skeletal muscle weakness and decrease muscle function. There are different types of muscular dystrophy. They share similar characteristics such as being hereditary, progressive and weakness. According to the National Institute of Neurological Disorders and...
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. The most common form is Duchenne...
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...
Introduction to Gene Therapy Gene therapy is an exciting new form of molecular medicine that introduces a functioning gene into a patient’s cells to compensate for abnormal genes and cure/alleviate the effects of a diseasing-causing mutation. Since its first success in 1990, gene therapy has...
Medical conditions concerning the muscles are difficult to manage even after research. The muscular system is incredibly complex, and its connections to the rest of body provide more issues when a disease is contracted. Muscular dystrophy is a medical condition that deconstructs the muscles in...
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