6
Views
0
CrossRef citations to date
0
Altmetric
Original Article

Heredity of mitochondrial ocular myopathy and Kearns Sayre syndrome

Pages 119-123 | Accepted 15 Oct 1990, Published online: 08 Jul 2009

References

  • Bastiaensen L AK. Chronic Progressive External Ophthalmoplegia. Stafleu Publ, Alphen a/d Rijn, Neth 1978
  • Bastiaensen L AK. On the heredity of mitochondrial cytopathies. Neuro-Ophthalmology 1987; 7: 151–157
  • Egger J, Wilson J. Mitochondrial inheritance in a mitochondrially mediated disease. New Engl J Med 1981; 309: 142–146
  • Holt I J, Harding A E, Cooper J M, et al. Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA. Ann Neurol 1989; 26: 1699–1708
  • Anderson S, Bankier A T, Barrell A G. Sequences and organization of the human mitochondrial genome. Nature 1981; 290: 457–465
  • Fine P EM. Mitochondrial inheritance and disease. Lancet 1978; ii: 659–662
  • Hutchinson C A, III, Newbold J E, Potter S E, et al. Maternal inheritance of human mitochondrial DNA. Nature 1970; 25: 536–538
  • Gittinger J W. Non myasthenic ophthalmoplegia. Current Neuro-Ophthalmology, S Lessell, J TW Van Dalen. Year Book Medical Publ Inc, Chicago 1990; Vol 2: 199–210
  • Holt I J, Harding A E, Morgan Hughes J A. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. Nature 1988; 331: 717–719
  • Zeviani M, Bonilla E, DeVivo D, DiMauro S. Mitochondrial diseases. Neurologic Clinics. Neurogenetic Diseases, W G Johnson. WB Saunders Cy, Philadelphia 1989; Vol 7: 123–156, No 1
  • Lestienne P, Ponsot G. Kearns Sayre syndrome with muscle mitochondrial DNA deletion. Lancet 1988; i: 885
  • Ozawa T, Yonada M, Tanaka M, et al. Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy. Biochem Biophys Res Comm 1988; 154: 1240–1247
  • Zeviani M, Moraes C T, DiMauro S, et al. Deletions of mitochondrial DNA in Kearns Sayre syndrome. Neurology 1988; 38: 1339–1346
  • Mita S, Schmidt B, Schon E A, et al. Deleted mitochondrial genomes in cytochrome-c-oxidase deficiency in ragged-red fibres of patients with Kearns Sayre syndrome. Ann Neurol 1989; 26: 123
  • Moraes C T, DiMauro S, Zeviani M, et al. Mitochondrial deletions in progressive external ophthalmoplegia and Kearns Sayre syndrome. New Engl J Med 1989; 320: 1293–1299
  • Shanske S, Moraes C T, Lombes A, et al. Widespread tissue distribution of mitochondrial DNA deletions in Kearns Sayre syndrome. Neurology 1990; 40: 24–27
  • Barré J A, Rohmer F. Surdité progressive, syndrome de Parinaud, troubles cérébelleux, dysréflexie vestibulaire croisée, chez un garcon de 16 ans. Troubles dégénératifs et ptosis chez plusieurs membres de la famille. Confin Neurol 1948; 8: 330–335

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.