常染色体優性遺伝性網膜色素変性症における新規N末端PRPF6バリアント
Na Li1,2, Yalong Dang1,2
1Department of Ophthalmology Sanmenxia Eye Hospital/Sanmenxia Central Hospital Affiliated to Henan University of Science and Technology Sanmenxia China.
Clinical case reports
|January 26, 2026
Abstract:
This report identifies the first N-terminal PRPF6 variant (c.514C>T) as a cause of autosomal dominant Retinitis Pigmentosa. This novel variant is associated with progressive peripheral vision loss but notably preserved central visual acuity, suggesting a distinct phenotypic expression compared to C-terminal variants.
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