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PATIENT REGISTRY (OLD)

The Patient Registry is for CANADIAN RESIDENTS ONLY. Are you living with an inherited retinal disease? Are you interested in helping to advance research in Canada and in contributing to the development...

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FBC FUNDED RESEARCH

Every year, donors of Fighting Blindness Canada (FBC) fund research taking place in hospitals and universities across Canada, and around the world. FBC and its generous supporters are currently committed to funding...

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X-LINKED RETINOSCHISIS

Jump to: Cause & Inheritance | Symptoms | Diagnosis | Treatment & Care | Research & Clinical Trials | Resources | References Overview X-linked retinoschisis (XLRS) is a rare genetic eye disease...

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USHER SYNDROME

Jump to: Causes & Inheritance | Symptoms| Diagnosis| Treatment & Care|Research & Clinical Trials| Resources overview Usher syndrome is a rare genetic condition that affects hearing and vision, and sometimes balance. It...

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STARGARDT DISEASE

Jump to: Causes & Inheritance|Symptoms| Diagnosis| Treatment & Care|Research & Clinical Trials | Resources | References Stargardt disease is an inherited retinal disease that causes progressive vision loss. It affects between 1...

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RETINITIS PIGMENTOSA

Jump to: Symptoms | Diagnosis | Treatments | Clinical Trials | RP Patient Registry | Research and Health Policy | Resources | References Overview Retinitis pigmentosa (RP) describes a group of genetic...

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