Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation.

Abstract:

:This report describes a multiple sclerosis (MS)-like disorder in a male patient with Leber's hereditary optic neuropathy (LHON) harbouring the mitochondrial DNA 11778 base pair mutation. Given the population frequencies of MS and LHON, coincidental occurrence is unlikely. Hypothetically the mitochondrial mutation underlying LHON may contribute to presumably immunologically mediated involvement of other myelinated axons in the central nervous system in susceptible individuals, producing a disorder indistinguishable from MS. We recommend that investigation for oligoclonal bands in CSF, evoked potentials and MR brain scan in these patients be supplemented with mitochondrial DNA analysis.

journal_name

Acta Neurol Scand

authors

Olsen NK,Hansen AW,Nørby S,Edal AL,Jørgensen JR,Rosenberg T

doi

10.1111/j.1600-0404.1995.tb07016.x

subject

Has Abstract

pub_date

1995-05-01 00:00:00

pages

326-9

issue

5

eissn

0001-6314

issn

1600-0404

journal_volume

91

pub_type

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