50 top medical experts on CblF Type Methylmalonic Aciduria and Homocystinuria across 6 countries and 2 U.S. states, including 12 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. CblF Type Methylmalonic Aciduria and Homocystinuria: cblF type methylmalonic acidemia with homocystinuria is a form of methylmalonic acidemia with homocystinuria (see this term), an inborn error of vitamin B12 (cobalamin) metabolism characterized by megaloblastic anemia, lethargy, failure to thrive, developmental delay, intellectual deficit and seizures.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Cobalamin F Disease,  Defect in Lysosomal Release of Cobalamin,  CblF Type Methylmalonic Acidemia and Homocystinuria,  Methylmalonic Aciduria due to Vitamin B12-Release Defect,  Vitamin B12 Lysosomal Release Defect,  Vitamin B12 Storage Disease


  

        

                    


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