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Kearns Syndrome

2 Diseases & Disorders / 2 Ocular Motility Disorders / 2 Ophthalmoplegia / 
2 Ophthalmoplegia, Chronic Progressive External / Kearns Syndrome

2 Diseases & Disorders / 2 Eye Diseases, Hereditary / 2 Retinitis Pigmentosa / 
Kearns Syndrome

2 Diseases & Disorders / 2 Retinal Diseases / 2 Retinal Degeneration / 
2 Retinitis Pigmentosa / Kearns Syndrome

 
  MeSH description: A mitochondrial disorder featuring the triad of chronic progressive external ophthalmoplegia, cardiomyopathy (with conduction block), and retinitis pigmentosa. Disease onset is in the first or second decade. Elevated CSF protein, sensorineural deafness, seizures, and pyramidal signs may also be present. Ragged-red fibers are found on muscle biopsy. (Adams et al., Principles of Neurology, 6th ed, p984)
 
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► Acta Estrabológica Órgano Oficial de la Sociedad Española de Estrabología -  Pleóptica, Ortóptica, Visión Binocular, Reeducación y Rehabilitación Visual. (in spanish).

► American Orthoptic Journal Official Journal of American Association of Certified Orthoptist. The journal serves as a forum for orthoptists and ophthalmologists to present clinical studies, reviews and new material in the fields of amblyopia, strabismus, and related areas of eye movement disorders.

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