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Laryngeal involvement in mitochondrial myopathy
Published online by Cambridge University Press: 29 June 2007
Abstract
A patient with a slowly progressive mitochondrial myopathy is presented. Mitochondrial myopathies are a diverse group of disorders both clinically and at the cellular level. In common with other neuromuscular disorders, bulbar symptoms may occur. However, though pharyngeal symptoms have been documented in all forms of the disorder, no previous account has described problems at the laryngeal level. We discuss the clinical findings and comment on the therapeutic options.
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References
Cros, D., Palliyath, S., DiMauro, S., Ramirez, C., Shamsnia, M., Wizer, B. (1992) Respiratory failure revealing mitochondrial myopathy in adults. Chest 101: 824–828.Google Scholar
DiMauro, S., Bonilla, E., Zeviani, M., Nakagawa, M., DeVivo, D. C. (1985) Mitochondrial myopathies. Annals of Neurology 17: 521–538.CrossRefGoogle ScholarPubMed
Fernandez-Sola, J., Casademont, J., Grau, J. M., Graus, E., Cardellach, F., Pedrol, E., Urbano-Marquez, A. (1992) Adult-onset mitochondrial myopathy. Postgraduate Medical Journal 68: 212–215.Google Scholar
Fourcin, A. J., Abberton, E. (1971) First applications of a new laryngograph. Medical and Biological Illustration 21: 172–182.Google ScholarPubMed
Friedmann, S., Goffin, F. B. (1966) Abductor vocal weakness in myasthenia gravis: report of a case. Laryngoscope 76: 1520–1523.Google Scholar
Hanson, D. G. (1991) Neuromuscular disorders of the larynx. Otolaryngologic Clinics of North America 24: 1035–1051.CrossRefGoogle ScholarPubMed
Harle, J.-R., Pellissier, J. -F., Desnouelle, C., Disdier, P., Figarella-Branger, D., Weiller, P. -J. (1992) Polymyalgia rheumatica and mitochondrial myopathy: clinicopathologic and biochemical studies in five cases. American Journal of Medicine 92: 167–172.Google Scholar
Kearns, T. P., Sayre, G. P. (1958) Retinitis pigmentosa, external ophthalmoplegia and complete heart block. Unusual syndrome with histologic study in one of two cases. Archives of Ophthalmology 60: 280–289.CrossRefGoogle ScholarPubMed
Luft, R., Ikkos, D., Palmieri, G., Ernster, L., Afzelius, B. (1962) A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical and morphological study. Journal of Clinical Investigation 41: 1776–1804.Google Scholar
Manni, R., Piccolo, G., Banfi, P., Ceveri, I., Bruschi, C., Zoia, C., Tartara, A. (1991) Respiratory patterns during sleep in mitochondrial myopathies with ophthalmoplegia. European Journal of Neurology 31: 12–17.Google Scholar
Pauzner, R., Blatt, I., Mouallem, M., Ben-David, E., Farfel, Z., Sadeh, M. (1991) Mitochondrial abnormalities in oculopharyngeal muscular dystrophy. Muscle and Nerve 14: 947–952.Google Scholar
Peyronnard, J.-M., Charron, L., Bellavance, A., Marchand, L. (1980) Neuropathy and mitochondrial myopathy. Annals of Neurology 7: 262–268.CrossRefGoogle ScholarPubMed
Schmidt-Nowara, W. W., Marder, E. J., Feil, P. A. (1984) Respiratory failure in myasthenia gravis due to vocal cord paresis. Archives of Neurology 41: 567–568.Google Scholar
Winter, P. H., Koopmann, C. F. (1990) Juvenile myasthenia gravis: an unusual presentation. International Journal of Pediatric Otorhinolaryngology 19: 273–276.Google Scholar
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