326 top medical experts on Homocystinuria across 39 countries and 22 U.S. states, including 172 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Homocystinuria: Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of cystathionine beta-synthase and associated with elevations of homocysteine in plasma and urine. Clinical features include a tall slender habitus, scoliosis, arachnodactyly, muscle weakness, genu varus, thin blond hair, malar flush, lens dislocations, an increased incidence of mental retardation, and a tendency to develop fibrosis of arteries, frequently complicated by cerebrovascular accidents and myocardial infarction. (From Adams et al., Principles of Neurology, 6th ed, p979)
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Connective Tissue Diseases (1,572), Hyperhomocysteinemia (1,066), Inborn Metabolic Brain Diseases (1,358).
  4. Clinical Trials ClinicalTrials.gov : at least 11 including 6 Completed, 4 Recruiting
  5. Synonyms: CBS Deficiency,  Cystathionine beta-Synthase Deficiency Disease


  

        

                    


    Computing Expert Listing ...

);