202 top medical experts on alpha-Mannosidosis across 26 countries and 7 U.S. states, including 17 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. alpha-Mannosidosis: An inborn error of metabolism marked by a defect in the lysosomal isoform of alpha-mannosidase activity that results in lysosomal accumulation of mannose-rich intermediate metabolites. Virtually all patients have psychomotor retardation, facial coarsening, and some degree of dysostosis multiplex. It is thought to be an autosomal recessive disorder.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Mannosidase Deficiency Diseases (22).
  4. Clinical Trials ClinicalTrials.gov : at least 22 including 3 Active, 9 Completed, 2 Recruiting
  5. Synonyms: Lysosomal alpha B Mannosidosis


  

        

                    


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