An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.
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 demons...
Main Authors: | Steckley, J, Ebers, G, Cader, M, McLachlan, R |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2001
|
Similar Items
-
A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia.
by: Cader, M, et al.
Published: (2005) -
Ondansetron for intractable vertigo complicating acute brainstem disorders.
by: Rice, G, et al.
Published: (1995) -
Genes for autosomal recessive cerebellar ataxia: order from chaos?
by: Nemeth, A, et al.
Published: (2001) -
Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).
by: George, A, et al.
Published: (1993) -
Urban vertigo
by: Lokting, Stanley W
Published: (2013)