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CNGA3-Related Achromatopsia: A 10-Year Follow-Up.
Haaris M Khan1, Fernando A G Sumita1,2, Rony Carlos Preti2
1Department of Ophthalmology and Vision Sciences, University of British Columbia, Vancouver, BC, Canada.
CNGA3-related achromatopsia shows progressive retinal changes on spectral-domain optical coherence tomography (SD-OCT) over 10 years, even with stable vision. This highlights SD-OCT
Area of Science:
- Ophthalmology
- Genetics
- Retinal Imaging
Background:
- CNGA3-related achromatopsia is a genetic retinal disorder.
- Traditionally viewed as a stationary condition.
- Long-term structural changes are not well-documented.
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