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Optic atrophy and cataract, autosomal dominant

Optic atrophy and cataract, autosomal dominant: Introduction

Optic atrophy and cataract, autosomal dominant: A very rare, dominantly inherited disorder characterized mainly by progressive optic nerve dysfunction, cataracts and neurological symptom. The neurological symptoms are usually very mild or don't even occur. More detailed information about the symptoms, causes, and treatments of Optic atrophy and cataract, autosomal dominant is available below.

Symptoms of Optic atrophy and cataract, autosomal dominant

Home Diagnostic Testing

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Wrongly Diagnosed with Optic atrophy and cataract, autosomal dominant?

Optic atrophy and cataract, autosomal dominant: Related Patient Stories

Causes of Optic atrophy and cataract, autosomal dominant

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Optic atrophy and cataract, autosomal dominant: Undiagnosed Conditions

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Misdiagnosis and Optic atrophy and cataract, autosomal dominant

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Optic atrophy and cataract, autosomal dominant: Research Doctors & Specialists

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Hospitals & Clinics: Optic atrophy and cataract, autosomal dominant

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Optic atrophy and cataract, autosomal dominant: Rare Types

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Optic atrophy and cataract, autosomal dominant: Animations

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Optic atrophy and cataract, autosomal dominant: Broader Related Topics

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Definitions of Optic atrophy and cataract, autosomal dominant:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Optic atrophy and cataract, autosomal dominant as a "rare disease".
Source - Orphanet

 

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