146 top medical experts on Limb-girdle muscular dystrophy type 2H across 15 countries and 8 U.S. states, including 12 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Limb-girdle muscular dystrophy type 2H: A mild subtype of autosomal recessive limb girdle muscular dystrophy characterized by slowly progressive proximal muscle weakness and wasting of the pelvic and shoulder girdles with onset that usually occurs during the second or third decade of life. Clinical presentation is variable and can include calf psuedohypertrophy, joint contractures, scapular winging, muscle cramping and/or facial and respiratory muscle involvement.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: LGMD2H,  Hutterite Type Muscular Dystrophy,  Type 2H Limb-Girdle Muscular Dystrophy,  Muscular dystrophy Hutterite type,  limb-girdle type 2H Muscular dystrophy,  Sarcotubular myopathy


  

        

                    


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