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...
Κύριοι συγγραφείς: | Steckley, J, Ebers, G, Cader, M, McLachlan, R |
---|---|
Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
2001
|
Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
-
A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia.
ανά: Cader, M, κ.ά.
Έκδοση: (2005) -
Editorial: Vertigo, tinnitus, and cognition
ανά: Xingxing Lu, κ.ά.
Έκδοση: (2024-05-01) -
Vestibular vertigo and ataxia in emergency neurology
ανά: Natalia Vladimirovna Aptikeeva, κ.ά.
Έκδοση: (2013-12-01) -
Nilotinib treatment outcomes in autosomal dominant spinocerebellar ataxia over one year
ανά: Woo-Jin Lee, κ.ά.
Έκδοση: (2024-07-01) -
Clinical Phenotypes of Autosomal Recessive Ataxias
ανά: J Gordon Millichap
Έκδοση: (2007-05-01)