Suppression of saccadic intrusions in hereditary ataxia by memantine.

نویسندگان

  • A Serra
  • K Liao
  • S Martinez-Conde
  • L M Optican
  • R J Leigh
چکیده

2008;70;810-812 Neurology A. Serra, K. Liao, S. Martinez-Conde, L. M. Optican and R. J. Leigh MEMANTINE SUPPRESSION OF SACCADIC INTRUSIONS IN HEREDITARY ATAXIA BY This information is current as of March 3, 2008 http://www.neurology.org/cgi/content/full/70/10/810 located on the World Wide Web at: The online version of this article, along with updated information and services, is All rights reserved. Print ISSN: 0028-3878. Online ISSN: 1526-632X. since 1951, it is now a weekly with 48 issues per year. Copyright © 2008 by AAN Enterprises, Inc. ® is the official journal of the American Academy of Neurology. Published continuously Neurology

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Ocular-Motor Profile and Effects of Memantine in a Familial Form of Adult Cerebellar Ataxia with Slow Saccades and Square Wave Saccadic Intrusions

Fixation instability due to saccadic intrusions is a feature of autosomal recessive spinocerebellar ataxias, and includes square wave intrusions (SWI) and macrosaccadic oscillations (MSO). A recent report suggested that the non-competitive antagonist of NMDA receptors, memantine, could decrease MSO and improve fixation in patients with spinocerebellar ataxia with saccadic intrusions (SCASI). We...

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Saccades during Attempted Fixation in Parkinsonian Disorders and Recessive Ataxia: From Microsaccades to Square-Wave Jerks

During attempted visual fixation, saccades of a range of sizes occur. These "fixational saccades" include microsaccades, which are not apparent in regular clinical tests, and "saccadic intrusions", predominantly horizontal saccades that interrupt accurate fixation. Square-wave jerks (SWJs), the most common type of saccadic intrusion, consist of an initial saccade away from the target followed, ...

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A form of inherited cerebellar ataxia with saccadic intrusions, increased saccadic speed, sensory neuropathy, and myoclonus.

Over the past five years, rapid progress has been made in genetically identifying different forms of spinocerebellar atrophy (SCA), for which several characteristic disorders of eye movements have been reported.1,2 Nonetheless, the genetic disorder in some families has not yet been discovered, and this report concerns one such kinship. We studied a family of Slovenian descent in which 5 of 14 s...

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Hereditary Ataxia with a Novel Mutation in the Senataxin Gene: A Case Report

Hereditary ataxias (HA) are a group of inherited neurological disorders caused by changes in genes. At least 115 different mutations in the senataxin (SETX) gene causing ataxia have been identified. There are no reports of any SETX gene mutation among the Iranian population. Here we report on two cases with homozygous and heterozygous mutations in which one patient was affected by HA with oculo...

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Characteristic Eye Movements in Ataxia-Telangiectasia-Like Disorder: An Explanatory Hypothesis

Objective To investigate cerebellar dysfunctions and quantitatively characterize specific oculomotor changes in ataxia-telangiectasia-like disorder (ATLD), a rare autosomal recessive disease caused by mutations in the MRE11 gene. Additionally, to further elucidate the pathophysiology of cerebellar damage in the ataxia-telangiectasia (AT) spectrum disorders. Methods Saccade dynamics, metrics, ...

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عنوان ژورنال:
  • Neurology

دوره 70 10  شماره 

صفحات  -

تاریخ انتشار 2008