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A mild form of POC1B-associated retinal dystrophy with relatively preserved cone system function
Takaaki Hayashi1,2, Kei Mizobuchi3, Shuhei Kameya4
1Department of Ophthalmology, The Jikei University School of Medicine, Tokyo, 105-8461, Japan. taka@jikei.ac.jp.
Documenta Ophthalmologica. Advances in Ophthalmology
|May 25, 2023
Summary
POC1B-associated retinopathy, a rare cause of cone dystrophy, can present with late-onset visual decline and relatively preserved cone function in older individuals. This case highlights a milder disease presentation than previously documented.
Area of Science:
- Ophthalmology
- Genetics
- Retinal Diseases
Background:
- Biallelic variants in POC1B are rare causes of autosomal recessive cone dystrophy.
- This condition is typically associated with generalized cone system dysfunction.
Keywords:
Autosomal recessive inheritanceCone dystrophyElectroretinographyOlder patientWhole-exome sequencingMore Related Videos
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