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Review
. 2003 May-Jun;37(3):713-20.

[Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like phenotype]

[Article in Polish]
Affiliations
  • PMID: 14593764
Review

[Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like phenotype]

[Article in Polish]
Zygmunt Jamrozik et al. Neurol Neurochir Pol. 2003 May-Jun.

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.

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