38 top medical experts on Actin-Accumulation Myopathy across 7 countries and 5 U.S. states, including 7 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Actin-Accumulation Myopathy: A rare, genetic, congenital myopathy disorder characterized by variable degrees of muscular weakness, frequently associated with severe nemaline myopathy-like disease (including neonatal hypotonia, lack of spontaneous movements, feeding and swallowing difficulties, frequent respiratory infections, respiratory insufficiency, early death), and histopathologic findings of large, densely packed, subsarcolemmal accumulations of thin, actin-immunopositive filaments (with or without intranuclear nemaline rods) on muscle biopsy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Actin Filament Aggregate Myopathy,  Actin Myopathy,  Congenital Myopathy with Excess of Thin Filaments,  With Cores Congenital Actin Myopathy,  With Intranuclear Rods Nemaline Myopathy 3,  Nemaline myopathy 3,  Nemaline myopathy caused by mutation in the alpha-actin gene


  

        

                    


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