Results 141 to 150 of about 9,115 (202)
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Persistent Corneal Defect in Chronic Progressive External Ophthalmoplegia
Journal of Medical Optometry, 2023This unique case highlights the difficulties of managing both CPEO and the complications related to the ocular surface and adnexa, including...
John Conto, Jane Bachman Groth
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Neurology
Chronic progressive external ophthalmoplegia (CPEO), a genetic syndrome characterized by slowly progressive paresis of extraocular muscles, is often due to single large-scale deletions of the mitochondrial genome (mtDNA).
Brian Y Li +6 more
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Chronic progressive external ophthalmoplegia (CPEO), a genetic syndrome characterized by slowly progressive paresis of extraocular muscles, is often due to single large-scale deletions of the mitochondrial genome (mtDNA).
Brian Y Li +6 more
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The Journal of craniofacial surgery (Print)
This report presents 2 cases of chronic progressive external ophthalmoplegia (CPEO) with progressive bilateral ptosis, managed successfully using Müller muscle-conjunctival resection with tarsectomy (MMCRT).
M. Mangan +3 more
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This report presents 2 cases of chronic progressive external ophthalmoplegia (CPEO) with progressive bilateral ptosis, managed successfully using Müller muscle-conjunctival resection with tarsectomy (MMCRT).
M. Mangan +3 more
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Chronic Progressive External Ophthalmoplegia
Archives of Ophthalmology, 1969The syndrome of chronic progressive external ophthalmoplegia has been generally regarded as denoting an ocular myopathy. Recent evidence is presented, however, which both denies the universality of a myopathic etiology and demonstrates our present inability to distinguish between myopathy and neural weakness of ocular muscles.
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Surgical management of ptosis in chronic progressive external ophthalmoplegia
European Journal of Ophthalmology, 2020Purpose: To determine possible complications and efficacy of ptosis surgery in a series of chronic progressive external ophthalmoplegia (CPEO) patients with healthy tear film.
M. Eshaghi, A. Arabi, Sarvin Eshaghi
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Journal of Neuromuscular Diseases, 2020
We describe a patient with chronic progressive external ophthalmoplegia (CPEO) due to a rare mitochondrial genetic variant. Muscle biopsy revealed numerous cytochrome c oxidase (COX)-deficient fibres, prompting sequencing of the entire mitochondrial ...
L. O'Donnell +9 more
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We describe a patient with chronic progressive external ophthalmoplegia (CPEO) due to a rare mitochondrial genetic variant. Muscle biopsy revealed numerous cytochrome c oxidase (COX)-deficient fibres, prompting sequencing of the entire mitochondrial ...
L. O'Donnell +9 more
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Journal of neuro-ophthalmology, 2020
C hronic progressive external ophthalmoplegia (CPEO) is a progressive neuromyopathic disorder marked by bilateral weakness of the levator and extraocular muscles, resulting in blepharoptosis and impaired ocular motility (1,2).
Christina Cherny +2 more
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C hronic progressive external ophthalmoplegia (CPEO) is a progressive neuromyopathic disorder marked by bilateral weakness of the levator and extraocular muscles, resulting in blepharoptosis and impaired ocular motility (1,2).
Christina Cherny +2 more
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Update on Chronic Progressive External Ophthalmoplegia
Strabismus, 2005Mitochondrial encephalomyopathies are clinically and genetically heterogeneous disorders. External ophthalmoplegia is the most frequent symptom. Other frequently involved tissues and organs include the retina, heart, limb muscles, peripheral and central nervous system, inner ear and endocrine system.
Viktoria, Bau, Stephan, Zierz
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Chronic Progressive External Ophthalmoplegia
American Orthoptic Journal, 2005IntroductionCredit for the first description in the literature regarding chronic progressive external ophthalmoplegia is generally attributed to von Graefe in 1868. Chronic progressive external ophthalmoplegia (CPEO) is a disorder that leads to complete immobility of the eyes.
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Chronic progressive external ophthalmoplegia.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 1998Two cases of chronic progressive external ophthalmoplegia were described. Both of them presented with progressive bilateral ptosis and gradual impairment of ocular mobility. One of the patients had abnormal cerebrospinal fluid protein level. Another patient had muscle biopsy which was compatible with mitochondrial myopathy.
K, Phanthumchinda +2 more
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