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. 2022 Oct;43(10):6117-6120.
doi: 10.1007/s10072-022-06193-7. Epub 2022 Jun 11.

MS diagnosis in a male patient with m.11778G > A Leber's hereditary optic neuropathy

Affiliations

MS diagnosis in a male patient with m.11778G > A Leber's hereditary optic neuropathy

Pasquale Scoppettuolo et al. Neurol Sci. 2022 Oct.
No abstract available

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References

    1. 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
    1. 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
    1. 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
    1. 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
    1. 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

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