113 top medical experts on Amish Infantile Epilepsy Syndrome across 6 countries and 10 U.S. states, including 18 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Amish Infantile Epilepsy Syndrome: GM3 synthase deficiency is a rare neurological disorder in which the brain does not develop normally. Symptoms of the disease begin within the first weeks or months of life and include difficulty feeding, irritability, vomiting, and seizures accompanied by loss of consciousness (grand mal seizures). Vision and hearing loss , spots of darker skin color (hyperpigmentation), and intellectual and developmental delays develop as the disease progresses.GM3 synthase deficiency is a congenital disorder of glycosylation and includes both cases described as Amish infantile epilepsy syndrome and cases described as salt & pepper syndrome.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: Infantile-Onset Symptomatic Epilepsy Syndrome,  GM3 Synthase Deficiency


  

        

                    


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