97 top medical experts on Hyperprolinemia type 2 across 10 countries and 4 U.S. states, including 7 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hyperprolinemia type 2: Hyperprolinemia type 2 is an autosomal recessive proline metabolism disorder due to pyroline-5-carboxylate dehydrogenase deficiency. The condition is often benign but clinical signs may include seizures, intellectual deficit and mild developmental delay.
  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: 1 alpha pyrroline-5-carboxylate dehydrogenase deficiency,  1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency,  Type II Hyperprolinemia,  Pyrroline Carboxylate Dehydrogenase Deficiency,  Pyrroline-5-Carboxylate Dehydrogenase Deficiency,  Type 2 hyperprolinemia


  

        

                    


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