81 top medical experts on Otodental Dysplasia across 6 countries, including 2 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Otodental Dysplasia: A contiguous gene syndrome comprising otodental syndrome (characterized by globodontia and sensorineural high-frequency hearing deficit) associated with eye abnormalities including, typically, iris and chorioretinal coloboma, as well as, on occasion, microcornea, microphtalmos, lenticular opacity, lens coloboma and iris pigment epithelial atrophy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Chromosome 11q13 Deletion Syndrome,  Oculootodental Syndrome,  Otodental Syndrome,  Otodental Syndrome With Coloboma


  

        

                    


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