206 top medical experts on Cogan type oculomotor Apraxia across 28 countries and 14 U.S. states, including 41 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Cogan type oculomotor Apraxia: Ocular motor apraxia, Cogan type is characterised by impairment of voluntary horizontal eye movements and compensatory head thrust. Around 50 cases have been described so far. The oculomotor manifestations tend to improve with age but the syndrome may also be associated with learning and speech difficulties, or, in some cases, cerebral malformations. Both sporadic and familial forms have been described, with sporadic forms being more frequent. The mode of transmission of the familial form has not yet been clearly established. A gene located on the long arm of chromosome 2, near to the NPHP1 gene involved in nephronophthisis, may be associated with ocular motor apraxia, Cogan type.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: type 2 Cogan's syndrome,  Congenital Oculomotor Apraxia,  Ocular Motor Apraxia,  Cogan Type Oculomotor Apraxia,  congenital Saccade initiation failure


  

        

                    


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