83 top medical experts on Vitreoretinochoroidopathy across 7 countries and 8 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. Vitreoretinochoroidopathy: A rare, genetic, vitreous-retinal disease characterized by ocular developmental anomalies such as microcornea, a shallow anterior chamber, glaucoma and cataract. Abnormal chorioretinal pigmentation is present, usually lying between the vortex veins and the ora serrata for 360 degrees.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: ADVIRC,  Autosomal dominant Vitreoretinochoroidopathy,  And Posterior Staphyloma Cataract Rod-Cone Dystrophy Microcornea,  And Cataract Glaucoma Vitreoretinochoroidopathy With Microcornea,  Vitreoretinochoroidopathy dominant,  Autosomal Dominant Vitreoretinochoroidopathy,  With Nanophthalmos Autosomal Dominant Vitreoretinochoroidopathy


  

        

                    


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