46 top medical experts on infantile histiocytoid Cardiomyopathy across 8 countries and 2 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. infantile histiocytoid Cardiomyopathy: A rare arrhythmogenic disorder characterized by cardiomegaly, severe cardiac arrhythmias or sudden death, and the presence of histiocyte-like cells within the myocardium.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Focal Lipid Cardiomyopathy,  Infantile Xanthomatous Cardiomyopathy,  Oncocytic Cardiomyopathy,  Foamy myocardial transformation of infancy,  Focal lipid cardiomyopathy,  Infantile xanthomatous cardiomyopathy,  Oncocytic cardiomyopathy


  

        

                    


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