| Literature DB >> 30898963 |
Nuno Moura-Coelho1,2, Rita Pinto Proença1, Joana Tavares Ferreira1,2, João Paulo Cunha1,2.
Abstract
Leber's hereditary optic neuropathy (LHON) is an optic neuropathy of mitochondrial inheritance, characterised by incomplete penetrance and variable expressivity. Typically, young male patients present with sequential, severe, rapidly progressive loss of central vision, with characteristic funduscopic findings. However, LHON may present at any age, in both genders, and fundus examination may be normal. Evidence has emerged to support the role of environmental factors in triggering LHON, by disrupting the normal mechanisms of mitochondrial function. We present two clinical cases of LHON of late onset, and provide a literature review on atypical cases of LHON and the role of environmental triggers. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: genetics; neuroopthalmology; ophthalmology; visual pathway
Mesh:
Year: 2019 PMID: 30898963 PMCID: PMC6453429 DOI: 10.1136/bcr-2018-227977
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X