MS diagnosis in a male patient with m.11778G > A Leber’s hereditary optic neuropathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-022-06193-7.pdf
Reference5 articles.
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
2. 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
3. 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
4. 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
5. 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
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