Arterial sheathing in Leber hereditary optic neuropathy.

Am J Ophthalmol Case Rep

Edward S. Harkness Eye Institute, Columbia University Irving Medical Center, New York, NY, USA.

Published: June 2022

AI Article Synopsis

  • A case study presents a 46-year-old woman with Leber hereditary optic neuropathy (LHON) who experienced a rapid loss of vision eleven years prior, with initial evaluations showing no arterial sheathing.
  • Genetic testing confirmed the LHON 11778 G-A mutation, and her vision deteriorated to count fingers at 12 feet, with significant retinal changes noted during examination.
  • The observations suggest that retinal arterial sheathing may be a rare feature of LHON, potentially expanding understanding of the condition's manifestations.

Article Abstract

Purpose: Presentation of a case of Leber hereditary optic neuropathy (LHON) with arterial sheathing eleven years after initial loss of vision.

Observations: A 46-year-old female was referred for re-evaluation of Leber hereditary optic neuropathy. She first noticed rapid painless loss of vision eleven years prior. Fundus imaging performed at that time did not demonstrate arterial sheathing. Genetic testing revealed the presence of the LHON 11778 G-A mitochondrial mutation. Laboratory values were within normal limits save for angiotensin-converting enzyme elevated to 69 U/L. Eleven years later, visual acuity was count fingers at 12 feet with complete loss of color vision. Funduscopic examination of the optic nerve revealed bilateral pallor, sheathing of the retinal arteries, diffuse vessel narrowing, and tortuous retinal vessels.

Conclusions And Importance: We present a case of LHON that demonstrates retinal arterial sheathing and possibly broadens the spectrum of LHON fundus findings.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881369PMC
http://dx.doi.org/10.1016/j.ajoc.2022.101431DOI Listing

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