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.
- 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.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: AICA Ribosuria due to ATIC Deficiency
Computing Expert Listing ...
Find Expert Doctors on AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency