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Original Article

Myotonic dystrophy mimicking bilateral internuclear ophthalmoplegia

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Pages 11-14 | Accepted 13 May 1996, Published online: 08 Jul 2009

References

  • Ashizawa T, Hejtmancik J F, Liu J, Perryman M B, Epstein H F, Koch D D. Diagnostic value of ophthalmologic findings in myotonic dystrophy: comparison with risks calculated by haplotype analysis of closely linked restriction fragment length polymorphisms. Am J Med Genet 1992; 42: 55–60
  • Aslanidis C, Jansen G, Ameniya C, Shutler G, Mahadevan M, Tsilfidis C, et al. Cloning of the essential myotonic dystrophy region and mapping of the putative defect. Nature 1992; 355: 548–551
  • Burian H, Burns C. Ocular changes in myotonic dystrophy. Am J Ophthalmol 1967; 63: 22–34
  • Junge J. Ocular changes in dystrophia myotonica, paramyotonia and myotonia congenita. Doc Ophthalmol 1966; 21: 1–115
  • Kerty E, Ganes T. Clinical and electrophysiological abnormalities in the visual system in myotonic dystrophy. Ophthalmologica 1989; 198: 95–102
  • Lessell S, Coppeto J, Samet S. Ophthalmoplegia in myotonic dystrophy. Am J Ophthalmol 1971; 71: 1231–1235
  • Koca M R, Horn F, Korth M. Alterations of saccadic eye movements in myotonic dystrophy. Graefe's Arch Clin Exp Ophthalmol 1992; 230: 437–441
  • Raitta C, Karli P. Ocular findings in myotonic dystrophy. Ann Ophthalmol 1982; 14: 647–650
  • Cogan D. Internuclear ophthalmoplegia, typical and atypical. Arch Ophthalmol 1970; 84: 583–589
  • Glaser J. Myasthenic pseudo-internu-clear ophthalmoplegia. Arch Ophthalmol 1966; 75: 363–366
  • Feldon S, Hoyt W, Stark L. Disordered inhibition in internuclear ophthalmoplegia. Analysis of eye movement recordings with computer simulations. Brain 1980; 103: 113–137
  • Buchthal F. (1977) Diagnostic significance of myopathic EMG. Pathogenesis of Human Muscular Dystrophies. Proceedings of the Fifth International Scientific Conference of the Muscular Dystrophy Association. 1977, L P Rowland. Excerpta Medica, Amsterdam, 10–19
  • Von Noorden G, Thompson H S, Van Allen M. Eye movements in myotonic dystrophy. An electrooculo-graphic study. Invest Ophthalmol Vis Sci 1964; 3: 314–322
  • Burns C. Ocular histopathology of myotonic dystrophy. A clinico-pathologic case report. Am J Ophthalmol 1969; 68: 416–422
  • Meyer E, Navon D, Auslender L, Zonis S. Myotonic dystrophy. Pathological study of the eyes. Ophthalmo-logica 1980; 181: 215–220
  • Kirkham T, Katsarkas A. An electro-oculographic study of internuclear ophthalmoplegia. Ann Neurol 1977; 2: 385–392
  • Metz H. Saccadic velocity measurements in internuclear ophthalmoplegia. Am J Ophthalmol 1976; 81: 296–299
  • Oohira A, Goto K, Ozawa T. Slow saccades in myogenic and peripheral neurogenic ophthalmoplegia. Latent ocular myopathy in myotonic dystrophy. Neuro-Ophthalmology 1985; 5: 117–123
  • Ter Bruggen J P, Bastiaensen A K, Tyssen C C, Gielen G. Disorders of eye movement in myotonic dystrophy. Brain 1990; 113: 463–473
  • Verhagen W IM, TerBruggen J P, Huygen P LM. Oculomotor, auditory, and vestibular responses in myotonic dystrophy. Arch Neurol 1992; 49: 954–969
  • Jamal G A, Weir A I, Hansen S, Ballantyne J P. Myotonic dystrophy: a reassessment by conventional and more recently introduced neurophysi-ological techniques. Brain 1986; 109: 1279–1296
  • Emre M, Henn V. Central eye movement disorder in a case of myotonic dystrophy. Neuro-Ophthalmology 1985; 5: 21–25

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