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Episodic ataxia

Reviewed August 2008

What is episodic ataxia?

Episodic ataxia is a group of related conditions that affect the nervous system and cause problems with movement. People with episodic ataxia have recurrent episodes of poor coordination and balance (ataxia). During these episodes, many people also experience dizziness (vertigo), nausea and vomiting, migraine headaches, blurred or double vision, slurred speech, and ringing in the ears (tinnitus). Seizures, muscle weakness, and paralysis affecting one side of the body (hemiplegia) may also occur during attacks. Additionally, some affected individuals have a muscle abnormality called myokymia during or between episodes. This abnormality can cause muscle cramping, stiffness, and continuous, fine muscle twitching that appears as rippling under the skin.

Episodes of ataxia and other symptoms can begin anytime from early childhood to adulthood. They can be triggered by environmental factors such as emotional stress, caffeine, alcohol, certain medications, physical activity, and illness. The frequency of attacks ranges from several per day to one or two per year. Between episodes, some affected individuals continue to experience ataxia, which may worsen over time, as well as involuntary eye movements called nystagmus.

Researchers have identified at least seven types of episodic ataxia, designated type 1 through type 7. The types are distinguished by their pattern of signs and symptoms, age of onset, length of attacks, and, when known, genetic cause.

How common is episodic ataxia?

Episodic ataxia is uncommon, affecting less than 1 in 100,000 people. Only types 1 and 2 have been identified in more than one family, and type 2 is by far the most common form of the condition.

What genes are related to episodic ataxia?

Episodic ataxia can be caused by mutations in several genes that play important roles in the nervous system. Three of these genes, KCNA1, CACNA1A, and CACNB4, provide instructions for making proteins that are involved in the transport of charged atoms (ions) across cell membranes. The movement of these ions is critical for normal signaling between nerve cells (neurons) in the brain and other parts of the nervous system. Mutations in the KCNA1, CACNA1A, and CACNB4 genes are responsible for episodic ataxia types 1, 2, and 5, respectively.

Mutations in the SLC1A3 gene have been found to cause episodic ataxia type 6. This gene provides instructions for making a protein that transports a brain chemical (neurotransmitter) called glutamate. Neurotransmitters, including glutamate, allow neurons to communicate by relaying chemical signals from one neuron to another.

Researchers believe that mutations in the KCNA1, CACNA1A, CACNB4, and SLC1A3 genes alter the transport of ions and glutamate in the brain, which causes certain neurons to become overexcited and disrupts normal communication between these cells. Although changes in chemical signaling in the brain underlie the recurrent attacks seen in people with episodic ataxia, it is unclear how mutations in these genes cause the specific features of the disorder.

The genetic causes of episodic ataxia types 3, 4, and 7 have not been identified. Researchers are looking for additional genes that can cause episodic ataxia.

Related Gene(s)

Changes in these genes are associated with episodic ataxia.

  • CACNA1A
  • CACNB4
  • KCNA1
  • SLC1A3

How do people inherit episodic ataxia?

This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder.

In some cases, an affected person inherits the mutation from one affected parent. Other cases result from new mutations in the gene and occur in people with no history of the disorder in their family.

Where can I find information about diagnosis or management of episodic ataxia?

These resources address the diagnosis or management of episodic ataxia and may include treatment providers.

  • Consortium for Clinical Investigations of Neurological Channelopathies (CINCH) (http://www.rarediseasesnetwork.org/cinch/)
  • Gene Review: Episodic Ataxia Type 1 (http://www.ncbi.nlm.nih.gov/books/NBK25442)
  • Gene Review: Episodic Ataxia Type 2 (http://www.ncbi.nlm.nih.gov/books/NBK1501)
  • Genetic Testing Registry: Episodic ataxia, type 3 (http://www.ncbi.nlm.nih.gov/gtr/conditions/C1847839)
  • Genetic Testing Registry: Episodic ataxia, type 4 (http://www.ncbi.nlm.nih.gov/gtr/conditions/C1847843)
  • Genetic Testing Registry: Episodic ataxia, type 7 (http://www.ncbi.nlm.nih.gov/gtr/conditions/C2677843)
  • Genetic Testing Registry: Episodic ataxia type 1 (http://www.ncbi.nlm.nih.gov/gtr/conditions/C1719788)
  • Genetic Testing Registry: Episodic ataxia type 2 (http://www.ncbi.nlm.nih.gov/gtr/conditions/C1720416)
  • MedlinePlus Encyclopedia: Movement - uncoordinated (http://www.nlm.nih.gov/medlineplus/ency/article/003198.htm)
  • MedlinePlus Encyclopedia: Vertigo-associated disorders (http://www.nlm.nih.gov/medlineplus/ency/article/001432.htm)

You might also find information on the diagnosis or management of episodic ataxia in Educational resources (http://ghr.nlm.nih.gov/condition/episodic-ataxia/show/Educational+resources) and Patient support (http://ghr.nlm.nih.gov/condition/episodic-ataxia/show/Patient+support).

General information about the diagnosis (http://ghr.nlm.nih.gov/handbook/consult/diagnosis) and management (http://ghr.nlm.nih.gov/handbook/consult/treatment) of genetic conditions is available in the Handbook. Read more about genetic testing (http://ghr.nlm.nih.gov/handbook/testing), particularly the difference between clinical tests and research tests (http://ghr.nlm.nih.gov/handbook/testing/researchtesting).

To locate a healthcare provider, see How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.

Where can I find additional information about episodic ataxia?

You may find the following resources about episodic ataxia helpful. These materials are written for the general public.

You may also be interested in these resources, which are designed for healthcare professionals and researchers.

What other names do people use for episodic ataxia?

  • EA

For more information about naming genetic conditions, see the Genetics Home Reference Condition Naming Guidelines (http://ghr.nlm.nih.gov/ConditionNameGuide) and How are genetic conditions and genes named? (http://ghr.nlm.nih.gov/handbook/mutationsanddisorders/naming) in the Handbook.

What if I still have specific questions about episodic ataxia?

Ask the Genetic and Rare Diseases Information Center (http://rarediseases.info.nih.gov/gard).

What glossary definitions help with understanding episodic ataxia?

ataxia ; autosomal ; autosomal dominant ; cell ; double vision ; gene ; hemiplegia ; inherited ; involuntary ; ions ; migraine ; mutation ; nervous system ; neuron ; neurotransmitters ; nystagmus ; protein ; stress ; tinnitus ; vertigo

You may find definitions for these and many other terms in the Genetics Home Reference Glossary (http://ghr.nlm.nih.gov/glossary).

References

  • Cader MZ, Steckley JL, Dyment DA, McLachlan RS, Ebers GC. A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia. Neurology. 2005 Jul 12;65(1):156-8. (http://www.ncbi.nlm.nih.gov/pubmed/16009908?dopt=Abstract)
  • Damji KF, Allingham RR, Pollock SC, Small K, Lewis KE, Stajich JM, Yamaoka LH, Vance JM, Pericak-Vance MA. Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias. Arch Neurol. 1996 Apr;53(4):338-44. Review. (http://www.ncbi.nlm.nih.gov/pubmed/8929156?dopt=Abstract)
  • Escayg A, De Waard M, Lee DD, Bichet D, Wolf P, Mayer T, Johnston J, Baloh R, Sander T, Meisler MH. Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia. Am J Hum Genet. 2000 May;66(5):1531-9. Epub 2000 Apr 4. (http://www.ncbi.nlm.nih.gov/pubmed/10762541?dopt=Abstract)
  • Gene Review: Episodic Ataxia Type 2 (http://www.ncbi.nlm.nih.gov/books/NBK1501)
  • Jen J, Kim GW, Baloh RW. Clinical spectrum of episodic ataxia type 2. Neurology. 2004 Jan 13;62(1):17-22. (http://www.ncbi.nlm.nih.gov/pubmed/14718690?dopt=Abstract)
  • Jen JC, Graves TD, Hess EJ, Hanna MG, Griggs RC, Baloh RW; CINCH investigators. Primary episodic ataxias: diagnosis, pathogenesis and treatment. Brain. 2007 Oct;130(Pt 10):2484-93. Epub 2007 Jun 15. Review. (http://www.ncbi.nlm.nih.gov/pubmed/17575281?dopt=Abstract)
  • Jen JC, Wan J, Palos TP, Howard BD, Baloh RW. Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures. Neurology. 2005 Aug 23;65(4):529-34. (http://www.ncbi.nlm.nih.gov/pubmed/16116111?dopt=Abstract)
  • Kerber KA, Jen JC, Lee H, Nelson SF, Baloh RW. A new episodic ataxia syndrome with linkage to chromosome 19q13. Arch Neurol. 2007 May;64(5):749-52. (http://www.ncbi.nlm.nih.gov/pubmed/17502476?dopt=Abstract)
  • Rajakulendran S, Schorge S, Kullmann DM, Hanna MG. Episodic ataxia type 1: a neuronal potassium channelopathy. Neurotherapeutics. 2007 Apr;4(2):258-66. Review. (http://www.ncbi.nlm.nih.gov/pubmed/17395136?dopt=Abstract)
  • Steckley JL, Ebers GC, Cader MZ, McLachlan RS. An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus. Neurology. 2001 Oct 23;57(8):1499-502. (http://www.ncbi.nlm.nih.gov/pubmed/11673600?dopt=Abstract)
  • Strupp M, Zwergal A, Brandt T. Episodic ataxia type 2. Neurotherapeutics. 2007 Apr;4(2):267-73. Review. (http://www.ncbi.nlm.nih.gov/pubmed/17395137?dopt=Abstract)

 

The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.

 
Reviewed: August 2008
Published: January 27, 2015