Literature DB >> 11796775

Ocular motor myotonic phenomenon in myotonic dystrophy.

M Versino1, B Rossi, G Beltrami, G Sandrini, V Cosi.   

Abstract

OBJECTIVE: To detect disconjugate ocular motor abnormalities and a possible extraocular muscle myotonic phenomenon in patients with myotonic dystrophy (MyD).
METHODS: The magnetic scleral search coil technique was used to record monocularly the small (25 degrees ) and large (50 degrees ) saccades, which were paced to two interstimulus intervals (ISIs), one short (1 s), the other long (5 s). The case study comprised 20 patients with MyD, 10 patients with multiple sclerosis (MS), and 10 controls. The amplitude, duration, peak velocity, and skewness of the velocity profile (ratio between the acceleration and the deceleration periods) of each saccade were measured. The disconjugate parameters (difference between the two eyes of the same measure), and the myotonic parameter (the maximal (as absolute value) short-long ISI difference between the same measures) were considered.
RESULTS: The disconjugate parameters were the same in all three groups. The mean values of myotonic parameters found in patients with MyD for duration (for both small and large target displacements) and skewness (for small target displacements only) differed from those found for both the MS and the control groups. Additionally, the occurrence of individual patients presenting with abnormal duration and skewness parameters was higher in the MyD than in the MS group. In patients with MyD, the saccade duration was longer for long than for short ISI; the effect derived from a prolongation of the acceleration period, which manifested as an increase in skewness.
CONCLUSION: The results can be explained by a combination of the myotonic and the warm up phenomena. A delay in the relaxation (myotonia) of the extraocular muscle may be more evident after a long fixation period (long ISI) and it may improve by increasing saccade pacing (short ISI-warm up). This phenomenon is slight, and is unlikely to affect saccade performance significantly, but it may provide some insight into the nature of the disorder affecting extraocular and skeletal muscles in myotonic dystrophy.

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Mesh:

Year:  2002        PMID: 11796775      PMCID: PMC1737732          DOI: 10.1136/jnnp.72.2.236

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  14 in total

1.  Small increase in triplet repeat length of cerebellum from patients with myotonic dystrophy.

Authors:  S Ishii; T Nishio; N Sunohara; T Yoshihara; K Takemura; K Hikiji; S Tsujino; N Sakuragawa
Journal:  Hum Genet       Date:  1996-08       Impact factor: 4.132

2.  THE EYE IN DYSTROPHIA MYOTONICA: WITH A REPORT ON ELECTROMYOGRAPHY OF THE EXTRA-OCULAR MUSCLES.

Authors:  S I Davidson
Journal:  Br J Ophthalmol       Date:  1961-03       Impact factor: 4.638

Review 3.  Myotonic dystrophy.

Authors:  J C Morgenlander; J M Massey
Journal:  Semin Neurol       Date:  1991-09       Impact factor: 3.420

4.  Physiological characterisation of the "warm up" effect of activity in patients with myotonic dystrophy.

Authors:  R G Cooper; M J Stokes; R H Edwards
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-09       Impact factor: 10.154

Review 5.  The myotonic dystrophies.

Authors:  C Thornton
Journal:  Semin Neurol       Date:  1999       Impact factor: 3.420

6.  Disorders of binocular control of eye movements in patients with cerebellar dysfunction.

Authors:  M Versino; O Hurko; D S Zee
Journal:  Brain       Date:  1996-12       Impact factor: 13.501

7.  Abnormalities of ocular motility in myotonic dystrophy.

Authors:  D Anastasopoulos; H Kimmig; T Mergner; K Psilas
Journal:  Brain       Date:  1996-12       Impact factor: 13.501

8.  Eye movements in myotonic dystrophy.

Authors:  E Bollen; J C den Heyer; M H Tolsma; S Bellari; J E Bos; A R Wintzen
Journal:  Brain       Date:  1992-04       Impact factor: 13.501

9.  Myotonic dystrophy: clinical assessment of muscular disability in an isolated population with presumed homogeneous mutation.

Authors:  J Mathieu; M De Braekeleer; C Prévost; C Boily
Journal:  Neurology       Date:  1992-01       Impact factor: 9.910

10.  Disorders of eye movement in myotonic dystrophy.

Authors:  J P Ter Bruggen; L A Bastiaensen; C C Tyssen; G Gielen
Journal:  Brain       Date:  1990-04       Impact factor: 13.501

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  1 in total

1.  In myotonic dystrophy type 1 reduced FDG-uptake on FDG-PET is most severe in Brodmann area 8.

Authors:  Dimitri Renard; Laurent Collombier; Christel Castelli; Jean-Pierre Pouget; Pierre-Olivier Kotzki; Vincent Boudousq
Journal:  BMC Neurol       Date:  2016-07-13       Impact factor: 2.474

  1 in total

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