50 top medical experts on beta-Mannosidosis across 8 countries and 4 U.S. states, including 6 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. beta-Mannosidosis: An inborn error of metabolism marked by a defect in the lysosomal isoform of beta-mannosidase that results in lysosomal accumulation of mannose-rich intermediate metabolites containing 1,4-beta linkages. The human disease occurs through autosomal recessive inheritance and manifests in the form of a variety of symptoms that depend upon the type of gene mutation.
  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 1
  5. Synonyms: Lysosomal beta A Mannosidosis


  

        

                    


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