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Figure 2

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Publication: Zhang et al., 2021 - SNRNP200 Mutations Cause Autosomal Dominant Retinitis Pigmentosa
All Figures: Figures for Zhang et al., 2021

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Figure 2

Clinical information of this adRP family. (A) Right eye fundus of the proband (III:1) presents characteristic RP degeneration, including a waxy pallor of optic disc, attenuated artery and vein and peripheral pigment deposit. (B) OCT scan reveals macular degeneration showing reduced thickness of outer nuclear layer (ONL) and RPE at the macular area with partial loss of outer/inner segments (OS/IS). (C,D) Fundus picture and Optical coherence tomography (OCT) scans of the left eye of the unaffected member (III:3) showing as normal controls. (E) Visual fields of the right eye of the proband indicates the tubular visual field.

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