202 top medical experts on Carnitine palmitoyl transferase 2 deficiency across 17 countries and 12 U.S. states, including 24 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Carnitine palmitoyl transferase 2 deficiency: Carnitine palmitoyltransferase II (CPT II) deficiency is an inherited metabolic disorder that affects mitochondrial oxidation of long chain fatty acids (LCFA). Three forms of CPT II deficiency have been described: a myopathic form, a severe infantile form and a neonatal form (see these terms).
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Carnitine Palmitoyltransferase 2 Deficiency,  Carnitine Palmitoyltransferase Ii Deficiency,  Carnitine palmitoyltransferase deficiency type 2,  Cpt Ii Deficiency,  Cpt2 Deficiency,  Muscle form of carnitine palmitoyltransferase deficiency


  

        

                    


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