44 top medical experts on Sarcosinemia across 7 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Sarcosinemia: A rare inborn error of metabolism characterized by increased concentrations of sarcosine in plasma and urine due to sarcosine dehydrogenase deficiency. The condition is considered benign and not associated with any specific clinical phenotype. Mode of inheritance is autosomal recessive.
  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: Hypersarcosinemia,  SARD Deficiency,  SARDH Deficiency,  deficiency of Sarcosin dehydrogenase complex,  Deficiency Of Sarcosine Dehydrogenase Complex


  

        

                    


    Computing Expert Listing ...