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Updated: May 18, 2026

Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo
Published on: September 22, 2017
Glaucoma progression associated with Leber's hereditary optic neuropathy.
Carlo Nucci1, Alessio Martucci, Raffaele Mancino
1Ophthalmological Unit, Department of Experimental Medicine and Surgery, University of Rome Tor Vergata, Via Montpellier 1, Rome, Italy. nucci@med.uniroma2.it
This case study highlights a patient with open-angle glaucoma whose condition rapidly worsened due to Leber's hereditary optic neuropathy. Genetic screening is recommended for glaucoma patients with unexplained vision loss.
Area of Science:
- Ophthalmology
- Genetics
- Neuroscience
Background:
- Open-angle glaucoma is a leading cause of irreversible blindness.
- Leber's hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disease.
- Both conditions affect the optic nerve and can lead to vision loss.
Observation:
- A 53-year-old female patient with pre-existing glaucoma experienced progressive visual field loss.
- Ophthalmological exams and blood tests ruled out other contributing diseases.
- Genetic testing identified a mitochondrial DNA mutation consistent with LHON.
Findings:
- The patient presented with the co-occurrence of open-angle glaucoma and LHON.
- This case suggests a potential cumulative effect of both conditions on retinal ganglion cell death.
- Rapid visual impairment progression was observed despite controlled intraocular pressure.
Implications:
- The combined effect of glaucoma and LHON may accelerate vision loss through increased oxidative stress.
- Consider genetic screening for mitochondrial DNA mutations in glaucoma patients with rapid, unexplained progression.
- This finding may inform diagnostic approaches and management strategies for complex optic neuropathies.
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