5 top medical experts on Infantile Carnitine Palmitoyltransferase II Deficiency across 1 countries, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Infantile Carnitine Palmitoyltransferase II Deficiency: The severe infantile form of carnitine palmitoyltransferase II (CPT II) deficiency (see this term), an inherited disorder that affects mitochondrial oxidation of long chain fatty acids (LCFA), is the early-onset form of the disease.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Hepatic CPT II Deficiency,  Infantile CPT2 Deficiency,  Carnitine Palmitoyltransferase II Deficiency with Hypoketotic Hypoglycemia,  Hepatocardiomuscular Carnitine Palmitoyltransferase II Deficiency


  

        

                    


    Computing Expert Listing ...