12 top medical experts on AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency across 1 countries, including 2 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency: A rare and severe inborn metabolic disease characterized clinically by the association of severe-to-profound neurodevelopmental impairment, severe visual impairment, ante-postnatal growth impairment, severe scoliosis and, frequently, early-onset epilepsy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: AICA Ribosuria due to ATIC Deficiency


  

        

                    


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