5 top medical experts on Kaeser Type Neurogenic Scapuloperoneal Syndrome across 0 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Kaeser Type Neurogenic Scapuloperoneal Syndrome: A rare, genetic, neuromuscular disease characterized by adult-onset muscle weakness and atrophy in a scapuloperoneal distribution, mild involvement of the facial muscles, dysphagia, and gynecomastia. Elevated serum CK levels and mixed myopathic and neurogenic abnormalities are associated clinical findings.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Kaeser Syndrome,  Stark-Kaeser Syndrome


  

        

                    


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