Find Expert Doctors on Early-onset ataxia with oculomotor apraxia and hypoalbuminemia97 top medical experts on Early-onset ataxia with oculomotor apraxia and hypoalbuminemia across 6 countries and 3 U.S. states, including 12 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Early-onset ataxia with oculomotor apraxia and hypoalbuminemia: A rare genetic disease characterized by slowly progressive cerebellar degeneration resulting in ataxia, oculomotor apraxia, and other cerebellar symptoms. There is an increased frequency of spontaneous chromosomal aberrations, as well as hypersensitivity to ionizing radiation, while telangiectasia is absent.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Support Organizations
- National Ataxia Foundation
600 Highway 169 South
Suite 1725
Minneapolis, MN 55426
Telephone: +1-763-553-0020
Fax: +1-763-553-0167
E-mail: naf@ataxia.org
Website: https://ataxia.org/
- Synonyms: With Oculomotor Apraxia Adult-Onset Ataxia, With Oculomotor Apraxia And Hypoalbuminemia Early-Onset Ataxia, Ataxia-oculomotor apraxia 1, Ataxia-oculomotor apraxia syndrome, Ataxia-telangiectasia-like syndrome, With Hypoalbuminemia Early-Onset Cerebellar Ataxia, Early-Onset Ataxia with Ocular Motor Apraxia and Hypoalbuminemia, Early-onset cerebellar ataxia with hypoalbuminemia
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