109 top medical experts on type 2C Limb-girdle muscular dystrophy across 10 countries and 3 U.S. states, including 8 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. type 2C Limb-girdle muscular dystrophy: A subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a childhood onset of progressive shoulder and pelvic girdle muscle weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. Mild to moderate elevated serum creatine kinase levels and positive Gowers sign are reported.
  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: secondary Adhalin deficiency,  type 1 autosomal recessive Duchenne-like muscular dystrophy,  Gamma-sarcoglycanopathy,  LGMD2C,  Limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency,  Maghrebian myopathy,  Type 2C Limb-Girdle Muscular Dystrophy,  Duchenne-like Muscular dystrophy,  SCARMD,  North African type Severe childhood autosomal recessive muscular dystrophy


  

        

                    


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