1,448
Views
20
CrossRef citations to date
0
Altmetric
Case Report

An Autopsy Case of Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) with Intestinal Bleeding in Chronic Renal Failure

, , , , , , , , , , , , , , , , & show all
Pages 622-625 | Received 26 Nov 2010, Accepted 01 May 2011, Published online: 01 Jun 2011

REFERENCES

  • DiMauro S, Moraes CT. Mitochondrial encephalomyopathies. Arch Neurol. 1993;50:1197–1208.
  • Goto Y, Nonaka I, Horai S. A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature. 1990;348: 651–653.
  • Petty RK, Harding AE, Morgan-Hughes JA. The clinical features of mitochondrial myopathy. Brain. 1986;109(5):915–938.
  • Tsujita Y, Kunitomo T, Fujii M, . A surviving case of mitochondrial cardiomyopathy diagnosed from the symptoms of multiple organ dysfunction syndrome. Int J Cardiol. 2008;128:e43–e45.
  • Mochizuki H, Joh K, Kawame H, . Mitochondrial encephalomyopathies preceded by de-Toni-Debre-Fanconi syndrome or focal segmental glomerulosclerosis. Clin Nephrol. 1996;46:347–352.
  • Ban S, Mori N, Saito K, Mizukami K, Suzuki T, Shiraishi H. An autopsy case of mitochondrial encephalomyopathy (MELAS) with special reference to extra-neuromuscular abnormalities. Acta Pathol Jpn. 1992;42:818–825.
  • Yoneda M, Tanaka M, Nishikimi M, . Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS). J Neurol Sci. 1989;92:143–158.
  • Yanagihara C, Oyama A, Tanaka M, Nakaji K, Nishimura Y. An autopsy case of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with chronic renal failure. Intern Med. 2001;40:662–665.
  • Barak Y, Arnon S, Wolach B, . MELAS syndrome: Peripheral neuropathy and cytochrome C-oxidase deficiency: A case report and review of the literature. Isr J Med Sci. 1995;31:224–229.
  • Matsushita T, Sano T, Nakano S, Matsuda H, Okada S. Successful mitral valve replacement for MELAS. Pediatr Neurol. 1993;9:391–393.
  • Suzuki S, Hinokio Y, Hirai S, . Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: A study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS). Diabetologia. 1994;37:818–825.
  • Kato H, Uchigata M, Iijima M, Shimizu S, Nonaka I, Goto Y. Fatal cerebral hemorrhage in mitochondrial encephalomyopathy. Clinical and pathological data of a case. J Neurol. 2006;253:529–530.
  • Kishnani PS, Van Hove JL, Shoffner JS, Kaufman A, Bossen EH, Kahler SG. Acute pancreatitis in an infant with lactic acidosis and a mutation at nucleotide 3243 in the mitochondrial DNA tRNALeu(UUR) gene. Eur J Pediatr. 1996;155:898–903.
  • Rubanyi GM, Vanhoutte PM. Superoxide anions and hyperoxia inactivate endothelium-derived relaxing factor. Am J Physiol. 1986;250:H822–H827.

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.