203 top medical experts on Lecithin Cholesterol Acyltransferase Deficiency across 17 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. Lecithin Cholesterol Acyltransferase Deficiency: An autosomal recessive disorder of lipoprotein metabolism caused by mutation of lecithin cholesterol acyltransferase gene. It is characterized by low HDL-cholesterol levels, and the triad of corneal opacities; hemolytic anemia; and proteinuria with renal failure.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Hypoalphalipoproteinemias (326).
  4. Clinical Trials ClinicalTrials.gov : at least 3 including 2 Completed


  

        

                    


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