MS diagnosis in a male patient with m.11778G > A Leber's hereditary optic neuropathy
- PMID: 35690699
- DOI: 10.1007/s10072-022-06193-7
MS diagnosis in a male patient with m.11778G > A Leber's hereditary optic neuropathy
References
-
- Nikoskelainen EK, Marttila RJ, Huoponen K et al (1995) Leber’s “plus”: Neurological abnormalities in patients with Leber’s hereditary optic neuropathy. J Neurol Neurosurg Psychiatry 59:160–164. https://doi.org/10.1136/jnnp.59.2.160 - DOI - PubMed - PMC
-
- Harding AE, Sweeney MG, Miller DH et al (1992) Occurrence of a multiple sclerosis-like illness in women who have a leber’s hereditary optic neuropathy mitochondrial dna mutation. Brain 115:979–989. https://doi.org/10.1093/brain/115.4.979 - DOI - PubMed
-
- Palace J (2009) Multiple sclerosis associated with Leber’s hereditary optic neuropathy. J Neurol Sci 286:24–27. https://doi.org/10.1016/j.jns.2009.09.009 - DOI - PubMed
-
- Cleaver J, Morrison H, Reynolds G et al (2021) Late-onset Leber’s hereditary optic neuropathy presenting with longitudinally extensive myelitis harbouring the m14484T>C mutation: extending the genotype-phenotype spectrum. Mult Scler Relat Disord 48:102688. https://doi.org/10.1016/j.msard.2020.102688 - DOI - PubMed
-
- Matthews L, Enzinger C, Fazekas F et al (2015) MRI in Leber’s hereditary optic neuropathy: the relationship to multiple sclerosis. J Neurol Neurosurg Psychiatry 86:537–542. https://doi.org/10.1136/jnnp-2014-308186 - DOI - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
