200 top medical experts on Ethylmalonic encephalopathy across 16 countries and 6 U.S. states, including 11 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Ethylmalonic encephalopathy: Ethylmalonic acid encephalopathy (EE) is defined by elevated excretion of ethylmalonic acid (EMA) with recurrent petechiae, orthostatic acrocyanosis and chronic diarrhoea associated with neurodevelopmental delay, psychomotor regression and hypotonia with brain magnetic resonance imaging (MRI) abnormalities.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: and Ethylmalonic Aciduria Petechiae Encephalopathy,  ethylmalonic Encephalopathy,  Epema Syndrome,  and ethylmalonic aciduria petechiae Syndrome of encephalopathy


  

        

                    


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