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Optic Atrophy 3, Autosomal Dominant

Optic Atrophy 3, Autosomal Dominant: Introduction

Optic Atrophy 3, Autosomal Dominant: A rare syndrome characterized mainly by progressive dysfunction of the optic nerve which results in vision impairment. Vision impairment ranges from moderate to severe. Type 3 is inherited in an autosomal dominant manner and is caused by a genetic defect on chromosome 19q13.2-q13.3. More detailed information about the symptoms, causes, and treatments of Optic Atrophy 3, Autosomal Dominant is available below.

Symptoms of Optic Atrophy 3, Autosomal Dominant

Home Diagnostic Testing

Home medical testing related to Optic Atrophy 3, Autosomal Dominant:

Wrongly Diagnosed with Optic Atrophy 3, Autosomal Dominant?

Optic Atrophy 3, Autosomal Dominant: Related Patient Stories

Causes of Optic Atrophy 3, Autosomal Dominant

Read more about causes of Optic Atrophy 3, Autosomal Dominant.

Optic Atrophy 3, Autosomal Dominant: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Optic Atrophy 3, Autosomal Dominant

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Optic Atrophy 3, Autosomal Dominant: Research Doctors & Specialists

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Optic Atrophy 3, Autosomal Dominant: Animations

Optic Atrophy 3, Autosomal Dominant: Broader Related Topics

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