Abstract #4007
            T 2 mapping and Single Voxel 1 H-MRS Detect Skeletal Muscle Involvement in Young Boys with Duchenne Muscular Dystrophy
                      Sean C Forbes                     1                    , Glenn A. Walter                     1                    , 						William Rooney                     2                    , Dah-Jyuu Wang                     3                    , 						William Triplett                     1                    , Rebecca Willcocks                     1                    , 						James Pollaro                     2                    , Barry Byrne                     1                    , 						Richard Finkel                     4                    , Barry Russman                     5                    , 						Erika Finanger                     5                    , Gihan Tennekoon                     3                    , 						Lee Sweeney                     6                    , and Krista Vandenborne                     1          
            
            1
           
           University of Florida, Gainesville, Florida, 
						United States,
           
            2
           
           Oregon 
						Health & Science University, Portland, Oregon, United 
						States,
           
            3
           
           Children's 
						Hospital of Philadelphia, Philadelphia, Pennsylvania, 
						United States,
           
            4
           
           Nemours 
						Childrens Hospital, Florida, United States,
           
            5
           
           Shriners 
						Hospital for Children, Portland, Oregon, United States,
           
            6
           
           University 
						of Pennsylvania, Philadelphia, Pennsylvania, United 
						States
          
            
          Duchenne muscular dystrophy (DMD) is characterized by 
						progressive muscle deterioration, loss of functional 
						abilities, and reduced life expectancy. Functional 
						deficits in muscle performance are often not observed in 
						DMD until after age 7, and therefore these functional 
						measures may not be sensitive for detecting disease 
						progression at a young age. In this study we observed 
						that MRI-T
          
           2
          
          and
          
           1
          
          H
          
           2
          
          O 
						T
          
           2
          
          derived using
          
           1
          
          H-MRS 
						were sensitive to muscle involvement at a young age (5-7 
						years) consistent with increased inflammation and muscle 
						damage in DMD.
         
				
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