219 top medical experts on Zellweger Syndrome across 31 countries and 20 U.S. states, including 48 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Zellweger Syndrome: An autosomal recessive disorder due to defects in peroxisome biogenesis which involves more than 13 genes encoding peroxin proteins of the peroxisomal membrane and matrix. Zellweger syndrome is typically seen in the neonatal period with features such as dysmorphic skull; muscle hypotonia; sensorineural hearing loss; visual compromise; seizures; progressive degeneration of the kidneys and the liver. Zellweger-like syndrome refers to phenotypes resembling the neonatal Zellweger syndrome but seen in children or adults with apparently intact peroxisome biogenesis.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Metabolic Brain Diseases (1,358), Kidney Diseases (3,539), Liver Diseases (3,550), Multiple Abnormalities (3,208), Peroxisomal Disorders (437).
  4. Clinical Trials ClinicalTrials.gov : at least 6 including 3 Completed, 2 Recruiting
  5. Synonyms: Cerebrohepatorenal Syndrome,  Zellweger-Like Syndrome


  

        

                    


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