5 top medical experts on Transcobalamin I Deficiency across 1 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Transcobalamin I Deficiency: A rare, genetic, benign disorder of cobalamin transport, due to variable degrees of transcobalamin I deficiency, characterized by mildly low to almost undetectable plasma transcobalamin I levels and slighly low to absent serum cobalamin levels. Normal methylmalonic acid and homocysteine serum values and absence of megaloblastic anemia are reported. No specific clinical manifestations are associated and patients are typically asymptomatic.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Cobalamin Pseudodeficiency due to Transcobalamin Deficiency,  Cobalamin R Binder Protein Deficiency,  Transcobalamin I Deficiency With Lactoferrin Deficiency


  

        

                    


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