204 top medical experts on Trifunctional Protein Deficiency With Myopathy And Neuropathy across 26 countries and 8 U.S. states, including 29 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Trifunctional Protein Deficiency With Myopathy And Neuropathy: A mitochondrial disorder of long chain fatty acid oxidation characterized in most patients by onset in infancy/ early childhood of hypoketotic hypoglycemia, metabolic acidosis, liver disease, hypotonia and, frequently, cardiac involvement with arrhythmias and/or cardiomyopathy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Deficiency Long Chain 3-Hydroxyacyl-CoA Dehydrogenase,  LCHAD Deficiency,  Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency,  Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency,  Long-Chain 3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency,  Long-Chain 3-OH Acyl-CoA Dehydrogenase Deficiency,  Mitochondrial Trifunctional Protein Deficiency,  TFP Deficiency,  Trifunctional Protein Deficiency,  Type 1 Trifunctional Protein Deficiency,  Type 2 Trifunctional Protein Deficiency


  

        

                    


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