66 top medical experts on Carnitine palmitoyl transferase 1A deficiency across 7 countries and 2 U.S. states, including 3 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Carnitine palmitoyl transferase 1A deficiency: Carnitine palmitoyltransferase 1A (CPT-1A) deficiency is an inborn error of metabolism that affects mitochondrial oxidation of long chain fatty acids (LCFA) in the liver and kidneys, and is characterized by recurrent attacks of fasting-induced hypoketotic hypoglycemia and risk of liver failure.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations

Organizations Providing General Support

  • Synonyms: CPT 1A Deficiency,  Type I Hepatic CPT Deficiency,  CPT I Deficiency,  Carnitine Palmitoyltransferase I Deficiency,  Carnitine Palmitoyltransferase IA Deficiency,  Carnitine palmitoyltransferase 1 deficiency,  Hepatic carnitine palmitoyltransferase 1 deficiency,  Liver Form of Carnitine Palmitoyltransferase Deficiency


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