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Oculomotor apraxia Cogan type
Other Names for this Disease
- Cogan's syndrome type 2
- Congenital oculomotor apraxia
- Saccade initiation failure congenital
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Organizations Supporting this Disease
Joubert Syndrome and Related Disorders Foundation
1415 West Ave.
Cincinnati, OH 45215
Telephone: (614) 864-1362
Social Networking Websites
- DNAandU.org is a Web site and blog that collects firsthand stories from people facing issues, making tough decisions, and using genomic (DNA) information in their own healthcare. Click on the link to learn from their experiences and/or submit your own story.
- RareShare is an online social hub dedicated to patients, families and healthcare professionals affected by rare medical disorders.