Literature DB >> 6848082

Bilateral optic neuropathy with remission in young men. Variation on a theme by Leber?

S Lessell, R L Gise, G B Krohel.   

Abstract

Five young men had painless, progressive, bilateral loss of central vision with late optic atrophy. One had a family history of Leber's optic neuropathy. After being functionally blind for four to 21 months, spontaneous improvement began leading to remarkable recovery of vision in all patients. We propose that these are cases of Leber's optic neuropathy in which an unusual capacity for recovery may have been related to a lack of microvascular abnormalities in the fundi.

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Year:  1983        PMID: 6848082     DOI: 10.1001/archneur.1983.04050010022005

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  3 in total

1.  Mitochondrial genetics: principles and practice.

Authors:  J M Shoffner; D C Wallace
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

2.  A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology.

Authors:  D Mackey; N Howell
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

3.  Visual electrophysiologic findings in patients from an extensive Brazilian family with Leber's hereditary optic neuropathy.

Authors:  Solange R Salomão; Adriana Berezovsky; Rafael E Andrade; Rubens Belfort; Valerio Carelli; Alfredo A Sadun
Journal:  Doc Ophthalmol       Date:  2004-03       Impact factor: 2.379

  3 in total

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