20 top medical experts on Hereditary Myopathy with Lactic Acidosis across 2 countries and 3 U.S. states, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hereditary Myopathy with Lactic Acidosis: A rare disease characterised by myopathy with severe exercise intolerance and deficiencies of skeletal muscle succinate dehydrogenase and aconitase.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Iron-Sulfur Cluster Deficiency Myopathy,  Myoglobinuria due to Abnormal Glycolysis,  Myopathy with Deficiency of ISCU,  Myopathy with Deficiency of Iron-Sulfur Cluster Assembly Enzyme,  Myopathy with Deficiency of Succinate Dehydrogenase and Aconitase,  Swedish Type Myopathy with Exercise Intolerance


  

        

                    


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