202 top medical experts on Norrie disease across 19 countries and 6 U.S. states, including 39 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Norrie disease: A rare developmental defect during embryogenesis characterized by abnormal retinal development with congenital blindness. Common associated manifestations include sensorineural hearing loss and developmental delay, intellectual disability and/or behavioral disorders.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations

Organizations Providing General Support

  • Synonyms: Anderson-Warburg Syndrome,  Atrophia bulborum hereditaria,  Congenital Progressive Oculo-Acoustico-Cerebral Degeneration,  Episkopi blindness,  Fetal Iritis Syndrome,  Norrie syndrome,  Norrie's Disease,  Norrie-Warburg syndrome,  Oligophrenia Microphthalmus,  Pseudoglioma,  Pseudoglioma Congenita,  Whitnall-Norman Syndrome


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