Hereditary Ataxia
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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?
Taylor A. Finseth
Advanced in Hereditary Ataxia
Advanced in Hereditary Ataxia

Aurora Neuroscience Innovation

2801 W Kinnickinnic River Pkwy, Ste 550, 
Milwaukee, WI 
Languages Spoken:
English
Offers Telehealth

Taylor Finseth is a Neurologist in Milwaukee, Wisconsin. Dr. Finseth is rated as an Advanced provider by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Camptocormism, Parkinson's Disease, Movement Disorders, and Conversion Disorder.

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, Olivopontocerebellar Atrophy, Spinocerebellar Ataxia Type 3, and Drug Induced Dyskinesia.

 
 
 
 
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Elite in Hereditary Ataxia
Elite in Hereditary Ataxia

Office

300 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.

What are the Latest Advances for Hereditary Ataxia?
Enhancing the Objective Assessment of Friedreich Ataxia Severity: A Multiview IMU-Based Approach.
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Reliable Objective Assessment of Friedreich Ataxia Through Isolation Forest-Based Anomaly Detection.
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...