ISSN: 2161-0533
						Shamim  Shaikh Mohiuddin
	
					    												College of Medicine, 
PO Box-2114, Dammam-31541
Slovak republic						                            
                            
						
 Review
												A Comprehensive Review Study on Muscular Dystrophy and its Associated Impact on Health and Individuals 						
Author(s): Basil  Alaniz, Turki  Alghamdi, Hassan  Alhaji, Hussain Alghalaf, Hamza  Aldossary, Khaled  Aldajani, Rakan  Alotaibi and Shamim  Shaikh MohiuddinBasil  Alaniz, Turki  Alghamdi, Hassan  Alhaji, Hussain Alghalaf, Hamza  Aldossary, Khaled  Aldajani, Rakan  Alotaibi and Shamim  Shaikh Mohiuddin             
						
												
				 Muscle dystrophy is a genetic muscle disease which leads to progressive loss of muscle mass and a weakened
musculoskeletal system. There are more than 30 types of muscular dystrophy which vary in severity, symptoms, and
causes but the major ones are nine types. Duchenne MD is the most common type of muscular dystrophy, and it
takes place in most of the cases around 50% of them. Usually, boys are more affected by Duchenne MD because of
mutations in X chromosome (X-linked recessive). However, females who carry mutated gene will have few
symptoms. If one of the genes responsible for producing and protecting the protein is impacted, Muscle Dystrophy
can be affected. The family history of muscular dystrophy and young aged boys are at higher risk of developing the
disease (Duchenne MD). However, it exists in all ages, races and both sexes. The general clinical feature of MD is a
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