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What is Optic atrophy, autosomal dominant?

What is Optic atrophy, autosomal dominant?

  • Optic atrophy, autosomal dominant: A very rare, dominantly inherited form of optic atrophy characterized mainly by progressive optic nerve dysfunction, impaired color vision and pale optic discs.

Optic atrophy, autosomal dominant: Introduction

Types of Optic atrophy, autosomal dominant:

Broader types of Optic atrophy, autosomal dominant:

What causes Optic atrophy, autosomal dominant?

Causes of Optic atrophy, autosomal dominant: see causes of Optic atrophy, autosomal dominant

What are the symptoms of Optic atrophy, autosomal dominant?

Symptoms of Optic atrophy, autosomal dominant: see symptoms of Optic atrophy, autosomal dominant

Onset of Optic atrophy, autosomal dominant: early childhood

Optic atrophy, autosomal dominant: Testing

Diagnostic testing: see tests for Optic atrophy, autosomal dominant.

Misdiagnosis: see misdiagnosis and Optic atrophy, autosomal dominant.

How is it treated?

Doctors and Medical Specialists for Optic atrophy, autosomal dominant: Medical Geneticist, Ophthalmologist ; see also doctors and medical specialists for Optic atrophy, autosomal dominant.
Treatments for Optic atrophy, autosomal dominant: see treatments for Optic atrophy, autosomal dominant

Name of Optic atrophy, autosomal dominant

Main name of condition: Optic atrophy, autosomal dominant

 

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