176
Views
11
CrossRef citations to date
0
Altmetric
Case Reports

Corneal endothelial dysfunction in Pearson syndrome

, , , &
Pages 55-57 | Received 02 May 2011, Accepted 17 Jul 2011, Published online: 21 Sep 2011

REFERENCES

  • Schon EA. Rearrangements of mitochondrial DNA. In: Holt I, ed. Genetics of Mitochondrial Diseases. Oxford, UK: Oxford University Press, 2003;111–124.
  • Simonsz HJ, Barlocher K, Rotig A. Kearns-Sayre’s syndrome developing in a boy who survived Pearson’s syndrome caused by mitochondrial DNA deletion. Doc Ophthalmol 1992;82:73–79.
  • Ribes A, Riudor E, Valcarel R, et al. Pearson syndrome: altered tricarboxylic acid and urea-cycle metabolites, adrenal insufficiency and corneal opacities. J Inher Metab Dis 1993;16:537–540.
  • Adamis AP, Filatov V, Tripathi BJ, et al. Fuchs’ endothelial dystrophy of the cornea. Surv Ophthalmol 1993;38:149–168.
  • Sherrard E, Novakovic P, Speedwell L. Age-related changes of the corneal endothelium and stroma as seen in vivo by specular microscopy. Eye 1987;1(2):197–203.
  • Flynn JT, Bachynski BN, Rodrigues MM, et al. Hyperglycemic acidotic coma and death in Kearns-Sayre syndrome. Trans Am Ophthalmol Soc 1985;83:131–161.
  • Ohkoshi K, Ishida N, Yamaguchi T, Kanki K. Corneal endothelium in a case of mitochondrial encephalomyopathy (Kearns-Sayre syndrome). Cornea 1989;8:210–214.
  • Chang TS, Johns DR, Stark WJ, et al. Corneal decompensation in mitochondrial ophthalmoplegia plus (Kearns-Sayre) syndrome. Cornea;1994May; 13(3):269–73.
  • Boonstra F, Claerhout I, Hol F, et al . Corneal decompensation in a boy with Kearns-Sayre syndrome. Ophthalmic Genet 2002;23(4):247–251.
  • Ohkoshi K, Ishida N, Yamaguchi T, et al. Corneal endothelium in a case of mitochondrial encephalomyopathy (Kearns-Sayre syndrome). Cornea 1989;8:210–214.
  • Chang TS, Johns DR, Stark WJ, et al. Corneal decompensation in mitochondrial ophthalmoplegia plus (Kearns-Sayre) syndrome. Cornea 1994;13(3):269–273.
  • Albin RL. Fuch’s corneal dystrophy in a patient with mitochondrial DNA mutations. J.Med Genet 1998;35:258–259
  • Zarnowski T, Jaksch M, Rejdak R, et al . Kearns-Sayre syndrome, abnormal corneal endothelium and normal tension glaucoma. Acta Ophthalmol Scand 2003;81(5):543–545.
  • Chang TS, Johns D, Walker D, et al . Ocular clinicopathologic study of the mitochondrial encephalomyopathy overlap syndromes. Arch Ophthalmol 1993;111(9):1254–1262.
  • Kerr DS. Protean manifestations of mitochondrial diseases: a mini review. J Pediat Hematol Onc 1997;19(4):279–286.
  • Rummelt V, Folberg R, Ionasescu V, et al. Ocular pathology of MELAS syndrome with mitochondrial DNA nucleotide 3243 point mutation. Ophthalmology 1993;100:1757–1766.
  • Zeviani M, Gellera C, Pannacci M, et al. Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies. Ann Neurol 1990;28:94–97.
  • Larsson N-G, Holme E, Kristiansson B, et al. Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome. Pediatr Res 1990;28:131.

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.