Retinal Investigation Using Optos OCT Device

Inclusion criteria

• Male or female participants 18 years of age or older who have full legal capacity to volunteer on the date the informed consent is signed.
• Participants who understand the study and patient information sheet and can follow the instructions.
• Participants who agree to participate in the study.
• Control group where no retinal abnormalities were detected as part of the standard basic ophthalmic examination.
• Participants with retinal disease in at least one eye including: Early dry age-related macular degeneration, late stage dry age-related macular degeneration specifically geographic atrophy, Wet age-related macular degeneration, Retinitis pigmentosa, Diabetic retinopathy and other macular atrophic diseases

Exclusion criteria

• Inability to understand written and verbal English sufficiently to comprehend the study and provide informed consent
• Ophthalmic disease other than condition under investigation.
• Participants unable to tolerate ophthalmic imaging.
• Cataract (unless deemed mild in the opinion of the investigator)
• Participants with significant ocular media not sufficiently clear to obtain acceptable OCT images.
• Diabetes (unless part of the diabetic eye disease group)
• Binocular visual acuity worse than 6/18
• Strabismus (squint)
• Age related macular degeneration groups: polypoidal choroidal vasculopathy
• Participants with photo sensitivity epilepsy, experience of seizures, or sensitivity to flickering light (based on self-report)
• Pregnant