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PMID: 15136697 Published · ppublish English Case Reports Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine.

Neurology ·Vol. 62 ·No. 9 ·2004-05-11 ·Pages 1623-5

Strupp M, Kalla R, Dichgans M, Freilinger T, Glasauer S, Brandt T

Abstract

Patients with episodic ataxia type 2 (EA2) can often be successfully treated with acetazolamide. The authors report three patients with EA2 (two with proven mutations in the CACNA1A gene) whose attacks were prevented with the potassium channel blocker 4-aminopyridine (4-AP; 5 mg tid). Attacks recurred after treatment was stopped; subsequent treatment alleviated the symptoms (mean follow-up time 6 months). These effects might be due to an improvement of the impaired functioning of Purkinje cells.

MeSH Terms
4-Aminopyridine/pharmacology,therapeutic use Acetazolamide/therapeutic use Adolescent Adult Ataxia/drug therapy,genetics,prevention & control Calcium Channels/genetics Humans Male Middle Aged Mutation Nystagmus, Pathologic/drug therapy,genetics Potassium Channel Blockers/pharmacology,therapeutic use Purkinje Cells/drug effects Treatment Outcome
Chemicals
Calcium Channels Potassium Channel Blockers 4-Aminopyridine Acetazolamide
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Strupp M
Department of Neurology, University of Munich, Germany. [email protected]
Kalla R
Dichgans M
Freilinger T
Glasauer S
Brandt T
Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
1526-632X
Published
2004-05-11
Pages
1623-5
Language
English
Region
United States
NLM ID
0401060
Subset
IM
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