Episodic ataxia type 3 (EA3)

Evidence-based neurology checklist on episodic ataxia type 3 (ea3): Genetics The genetic mutation is unknown It is related to chromosome 1q The episodes last minutes to 6 hours Clinical features Treatment

Genetics

  • The genetic mutation is unknown
  • It is related to chromosome 1q
  • The episodes last minutes to 6 hours

Clinical features

Treatment

References

  1. Jen JC, Graves TD, Hess EJ, et al. Primary episodic ataxias: diagnosis, pathogenesis and treatment. Brain 2007; 130:2484-2493.
  2. Choi KD, Choi JH. Episodic ataxias: clinical and genetic features. J Mov Disord 2016; 9:129-135.
  3. 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; 65:156-158.
  4. Steckley JL, Ebers GC, Cader MZ, McLachlan RS. An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus. Neurology 2001; 57:1499-1502.

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