Different types of intra-saccadic slowing in congenital (RAPSN-mutation) and acquired myasthenic syndromes

H. Rambold*, T. Sander, C. Helmchen, W. Heide

*Korrespondierende/r Autor/-in für diese Arbeit
3 Zitate (Scopus)

Abstract

Saccadic slowing and saccadic fatigue is a common clinical finding in myasthenia gravis [1]. However, previous studies on eye movements in myasthenia gravis did not dissociate congenital (CMS) from acquired forms with acetylcholine‐receptor (ACHR) auto‐antibodies [1]. Therefore, saccades of one patient with CMS caused by two compound heterozygote mutations (N88K and 1177 del AA) in the RAPSN gene (2) (one mutation from each parent) were compared with three patients with acquired myasthenia gravis and two healthy controls.
OriginalspracheEnglisch
ZeitschriftEuropean Journal of Neurology
Jahrgang13
Ausgabenummer10
ISSN1351-5101
DOIs
PublikationsstatusVeröffentlicht - 01.10.2006

Strategische Forschungsbereiche und Zentren

  • Forschungsschwerpunkt: Gehirn, Hormone, Verhalten - Center for Brain, Behavior and Metabolism (CBBM)

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