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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.
Publication status:
Published

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Publisher copy:
10.1212/wnl.57.8.1499

Authors


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Institution:
University of Oxford
Department:
Oxford, MSD, Clinical Neuroscience, WTC Human Genetics
Role:
Author
More by this author
Institution:
University of Oxford
Department:
Oxford, MSD, Clinical Neuroscience, Molecular Medicine
Role:
Author
Journal:
Neurology
Volume:
57
Issue:
8
Pages:
1499-1502
Publication date:
2001-10-05
DOI:
EISSN:
1526-632X
ISSN:
0028-3878
URN:
uuid:a8e9c0d6-2426-4f05-afad-3edeb026b1ee
Source identifiers:
31982
Local pid:
pubs:31982

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