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Learn About Hereditary Ataxia

Condition 101 content is not available at this time, but we are continually updating the site. Please check back.

However, there may be experts who have treated this or similar conditions in our Find a Doctor section and research may be available in our Latest Advances section.

Who are the top Hereditary Ataxia Local Doctors?
Elite in Hereditary Ataxia
Elite in Hereditary Ataxia
Sao Paulo, SP, BR 

Jose Pedroso practices in Sao Paulo, Brazil. Mr. Pedroso is rated as an Elite expert by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Spinocerebellar Ataxia Type 3, Spinocerebellar Ataxia, Olivopontocerebellar Atrophy, and Drug Induced Dyskinesia.

Elite in Hereditary Ataxia
Elite in Hereditary Ataxia

The Regents Of The University Of California

150 Medical Plz, 
Los Angeles, CA 
Languages Spoken:
English
Offers Telehealth

Susan Perlman is a Neurologist in Los Angeles, California. Dr. Perlman is rated as an Elite provider by MediFind in the treatment of Hereditary Ataxia. Her top areas of expertise are Spinocerebellar Ataxia, Friedreich Ataxia, Drug Induced Dyskinesia, and Olivopontocerebellar Atrophy.

 
 
 
 
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Elite in Hereditary Ataxia
Elite in Hereditary Ataxia
50 Flemington Road, 
Parkville, VIC, AU 

Martin Delatycki practices in Parkville, Australia. Mr. Delatycki is rated as an Elite expert by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Friedreich Ataxia, Spinocerebellar Ataxia, Drug Induced Dyskinesia, and Hereditary Ataxia.

What are the latest Hereditary Ataxia Clinical Trials?
Phenotype/Genotype Correlations in Movement Disorders

Summary: The goal of this protocol is to identify families with inherited movement disorders and evaluate disease manifestations to establish an accurate clinical diagnosis by using newest technological advances and investigate the underlying molecular mechanisms. Studies of inherited movement disorders in large families with good genealogical records are especially valuable. Patients with diseases of know...

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Natural History of Spinocerebellar Ataxia Type 7 (SCA7)

Background: Spinocerebellar ataxia type 7 (SCA7) is a disease in which people have problems with coordination, balance, speech and vision. It is caused by a change in the ATXN7 gene. A mutation in this ATXN7 gene causes changes in eye cells, which can lead to vision loss. There is no cure for SCA7 but researchers are looking for possible treatments. Researchers need more information about SCA7. They want to c...