6 top medical experts on Autosomal Recessive Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions across 1 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Autosomal Recessive Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions: A rare genetic, neuro-ophthalmological disease characterized by progressive weakness of the external eye muscles, resulting in bilateral ptosis and diffuse, symmetric ophthalmoparesis. Additional signs may include generalized skeletal muscle weakness, muscle atrophy, sensory axonal neuropathy, ataxia, cardiomyopathy, and psychiatric symptoms. It is usually more severe than autosomal dominant form.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Autosomal Recessive Progressive External Ophthalmoplegia


  

        

                    


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