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Graefe's Archive for Clinical and Experimental Ophthalmology

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01-06-2018 | Letter to the Editor

Polymegathism as a biomarker of mitochondrial disorders

Authors: Josef Finsterer, Sinda Zarrouk-Mahjoub

Published in: Graefe's Archive for Clinical and Experimental Ophthalmology | Issue 6/2018

Excerpt

Letter to the Editor …

Bakhoum MF, Wu WP, White EC et al. (2018) Mitochondrial A3243G mutation results in corneal endothelial polymegathism. Graefes Arch Clin Exp Ophthalmol doi: https://doi.org/10.1007/s00417-018-3914-z

Finsterer J, Zarrouk-Mahjoub S (2017) Mitochondrial multiorgan disorder syndrome score generated from definite mitochondrial disorders. Neuropsychiatr Dis Treat 13:2569–2579CrossRefPubMedPubMedCentral

Anbar M, Ammar H, Mahmoud RA. (2016) Corneal endothelial morphology in children with type 1 diabetes. J Diabetes Res 2016:7319047. doi: https://doi.org/10.1155/2016/7319047

Rummelt V, Folberg R, Ionasescu V et al (1993) Ocular pathology of MELAS syndrome with mitochondrial DNA nucleotide 3243 point mutation. Ophthalmology 100:1757–1766CrossRefPubMed

Poulton J, Finsterer J, Yu-Wai-Man P (2017) Genetic counselling for maternally inherited mitochondrial disorders. Mol Diagn Ther 21:419–429CrossRefPubMed

Finsterer J, Bindu PS (2015) Therapeutic strategies for mitochondrial disorders. Pediatr Neurol 52:302–313CrossRefPubMed

Title: Polymegathism as a biomarker of mitochondrial disorders
Authors: Josef Finsterer
Sinda Zarrouk-Mahjoub
Publication date: 01-06-2018
Publisher: Springer Berlin Heidelberg
Published in: Graefe's Archive for Clinical and Experimental Ophthalmology / Issue 6/2018
Print ISSN: 0721-832X
Electronic ISSN: 1435-702X
DOI: https://doi.org/10.1007/s00417-018-3960-6

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Polymegathism as a biomarker of mitochondrial disorders

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