[Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like phenotype]
- PMID: 14593764
[Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like phenotype]
Abstract
A sporadic case of a 31 year-old woman with genetically confirmed diagnosis of LHON was presented. Both her optic nerves were affected, with a 5-year interval between the onset in one eye and the loss of vision in the second one. Besides optic atrophy clinical and laboratory signs of multiple sclerosis were found. A review of the literature suggests that the G3460A mutation present in this case rarely coexists with a MS-like clinical phenotype.
Similar articles
-
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.Mult Scler. 2011 Jun;17(6):763-6. doi: 10.1177/1352458511404033. Mult Scler. 2011. PMID: 21685233
-
Leber's optic neuropathy associated with disseminated white matter disease: a case report and review.Clin Neurol Neurosurg. 2009 Jan;111(1):83-6. doi: 10.1016/j.clineuro.2008.06.021. Epub 2008 Oct 9. Clin Neurol Neurosurg. 2009. PMID: 18848389 Review.
-
A case of neuromyelitis optica harboring both anti-aquaporin-4 antibodies and a pathogenic mitochondrial DNA mutation for Leber's hereditary optic neuropathy.Mult Scler. 2014 Feb;20(2):258-60. doi: 10.1177/1352458513513057. Epub 2013 Nov 21. Mult Scler. 2014. PMID: 24263387
-
Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.Eur Neurol. 2004;51(2):68-71. doi: 10.1159/000075518. Epub 2003 Dec 10. Eur Neurol. 2004. PMID: 14671420
-
Multiple sclerosis associated with Leber's Hereditary Optic Neuropathy.J Neurol Sci. 2009 Nov 15;286(1-2):24-7. doi: 10.1016/j.jns.2009.09.009. Epub 2009 Oct 1. J Neurol Sci. 2009. PMID: 19800080 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical