200 top medical experts on Familial Exudative Vitreoretinopathies across 13 countries and 15 U.S. states, including 51 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Familial Exudative Vitreoretinopathies: A group of inherited disorders characterized by incomplete development of the retinal vasculature. Its severity can vary from complete blindness in infancy, to mild or no visual problems, where small areas of vascular defects are observable only by fluorescein angiography. Exudative vitreoretinopathy 1 is associated with mutations in the FZD4 gene.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Hereditary Eye Diseases (901), Eye Abnormalities (1,966).
  4. Clinical Trials ClinicalTrials.gov : at least 2 including 1 Completed
  5. Synonyms: X-Linked Familial Exudative Vitreoretinopathy,  XL-FEVR


  

        

                    


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