204 top medical experts on Chanarin-Dorfman Syndrome across 21 countries and 7 U.S. states, including 18 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Chanarin-Dorfman Syndrome: A form of neutral lipid storage disease characterized by the accumulation of lipid vacuoles in leukocytes (so-called Jordan's anomaly seen in peripheral blood smears) and a variety of other cell types. The clinical picture consists of congenital ichthyosis of the congenital ichthyosiform erythroderma type together with variable multisystem involvement. Manifestations include hepatosplenomegaly, myopathy, intestinal disease, growth retardation, cataracts, sensorineural hearing loss, and intellectual disability, among others.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Chanarin-Dorfman disease,  Dorfman Chanarin syndrome,  Dorfman-Chanarin Syndrome,  Ichthyosiform erythroderma with leukocyte vacuolation,  Ichthyotic neutral lipid storage disease,  Neutral Lipid Storage Disease With Ichthyosis,  Neutral lipid storage myopathy,  Triglyceride Storage Disease with Ichthyosis,  Triglyceride storage disease with impaired long-chain fatty acid oxidation


  

        

                    


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