Oculomotor apraxia Cogan type
Other Names for this Disease
- Congenital oculomotor apraxia
- Cogan's syndrome type 2
- Saccade initiation failure congenital
- Ocular motor apraxia, Cogan type
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Unfortunately, there is no cure for oculomotor apraxia Cogan type and treatment is focused on managing symptoms. Vision therapies may be helpful for some children with this condition. It is recommended that individuals with this disorder see the appropriate specialists necessary to help monitor their specific symptoms. Suggested specialists may include a nephrologist (kidney specialist), ophthalmologist (eye doctor), geneticist, and neurologist, as well as any others recommended by your doctor. Kidney failure usually develops in childhood or early adulthood, and management may require medications, dialysis, and/or kidney transplantation.
Last updated: 3/25/2014
- Cogan type Congenital Oculomotor Apraxia. Joubert Syundrome and Related Disorders Foundation. http://www.jsrdf.org/PDF/cogansyndrome06-26-061.pdf. Accessed 3/24/2014.
- Finding Treatment Information - A video developed by GARD Information Specialists that explains how you can find information about treatment for a rare disease.
- The Centers for Mendelian Genomics program is working to discover the causes of rare genetic disorders. For more information about applying to the research study, please visit their website.
- ClinicalTrials.gov lists trials that are studying or have studied Oculomotor apraxia Cogan type. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.