An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.

Abstract:

:The authors report an autosomal dominant episodic ataxia that is clinically distinct from the other episodic ataxias. Vestibular ataxia, vertigo, tinnitus, and interictal myokymia are prominent; attacks are diminished by acetazolamide. Linkage analyses of markers flanking the EA1 and EA2 loci demonstrate genetic exclusion from the other autosomal dominant episodic ataxias. The authors suggest EA3 for periodic vestibulocerebellar ataxia and EA4 for the disorder described here.

journal_name

Neurology

journal_title

Neurology

authors

Steckley JL,Ebers GC,Cader MZ,McLachlan RS

doi

10.1212/wnl.57.8.1499

subject

Has Abstract

pub_date

2001-10-23 00:00:00

pages

1499-502

issue

8

eissn

0028-3878

issn

1526-632X

journal_volume

57

pub_type

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