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spinocerebellar ataxia type 2

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

A subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by truncal ataxia, dysarthria, slowed saccades and less commonly ophthalmoparesis and chorea.

Synonyms

  • ALS13
  • ATXN2 autosomal dominant cerebellar ataxia type I
  • OPCA2
  • SCA 2
  • SCA2
  • Wadia swami syndrome
  • Wadia-swami syndrome
  • amyotrophic lateral sclerosis 13
  • amyotrophic lateral sclerosis type 13
  • amyotrophic lateral sclerosis, susceptibility to, 13
  • autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2
  • cerebellar Degeneration with slow eye movements
  • olivopontocerebellar atrophy 2
  • olivopontocerebellar atrophy Holguin type
  • olivopontocerebellar atrophy, Holguin type
  • spinocerebellar Degeneration with slow eye movements
  • spinocerebellar ataxia 2
  • spinocerebellar ataxia Cuban type
  • spinocerebellar ataxia type 2
  • spinocerebellar ataxia with slow eye movements
  • spinocerebellar ataxia, Cuban type
  • spinocerebellar atrophy 2
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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