Yonsei Med J.  2019 Feb;60(2):230-231. 10.3349/ymj.2019.60.2.230.

Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA Deletions

• Finsterer

• KMID: 2431641
• DOI: http://doi.org/10.3349/ymj.2019.60.2.230

Abstract

No abstract available.

MeSH Terms

DNA, Mitochondrial*
Ophthalmoplegia*
DNA, Mitochondrial

Reference

1. Lee SJ, Na JH, Han J, Lee YM. Ophthalmoplegia in mitochondrial disease. Yonsei Med J. 2018; 59:1190–1196.

2. Krishna MR. Kearns Sayre Syndrome: looking beyond A-V conduction. Indian Pacing Electrophysiol J. 2017; 17:78–80.

3. Paramasivam A, Meena AK, Pedaparthi L, Jyothi V, Uppin MS, Jabeen SA, et al. Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging. Mitochondrion. 2016; 26:81–85.

4. Finsterer J, Zarrouk-Mahjoub S. Kearns-Sayre syndrome is genetically and phenotypically heterogeneous. Pediatr Med Chir. 2018; 40:193.