210 top medical experts on Visceral myopathy familial external ophthalmoplegia across 25 countries and 9 U.S. states, including 30 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Visceral myopathy familial external ophthalmoplegia: Mitochondrial NeuroGastroIntestinal Encephalomyopathy (MNGIE) syndrome is characterized by the association of gastrointestinal dysmotility, peripheral neuropathy, chronic progressive external ophthalmoplegia and leukoencephalopathy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Intestinal pseudoobstruction with external ophthalmoplegia,  MNGIE Disease,  MNGIE Syndrome,  Mitochondrial DNA Depletion Syndrome 1,  Mitochondrial DNA Depletion Syndrome 8A,  Autosomal Recessive With Renal Tubulopathy Encephalomyopathic Form Mitochondrial Dna Depletion Syndrome,  and Pseudo-Obstruction Ophthalmoplegia Mitochondrial Myopathy with Sensorimotor Polyneuropathy,  Mitochondrial Neurogastrointestinal Encephalopathy Disease,  Rrm2b-Related Mitochondrial Neurogastrointestinal Encephalopathy Syndrome,  Mitochondrial neurogastrointestinal encephalopathy syndrome,  Mngie Without Leukoencephalopathy,  Rrm2b-Related Mngie,  oculogastrointestinal Muscular dystrophy,  Myoneurogastrointestinal encephalopathy syndrome,  Oculogastrointestinal Muscular Dystrophy,  POLIP Syndrome,  and Intestinal Pseudo-Obstruction Leukoencephalopathy Ophthalmoplegia Polyneuropathy,  and intestinal pseudoobstruction leukoencephalopathy ophthalmoplegia Polyneuropathy,  Thymidine Phosphorylase Deficiency,  With External Ophthalmoplegia Familial Visceral Myopathy


  

        

                    


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