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Optic atrophy, autosomal dominant

Optic atrophy, autosomal dominant: Introduction

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. More detailed information about the symptoms, causes, and treatments of Optic atrophy, autosomal dominant is available below.

Symptoms of Optic atrophy, autosomal dominant

Home Diagnostic Testing

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Wrongly Diagnosed with Optic atrophy, autosomal dominant?

Causes of Optic atrophy, autosomal dominant

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Optic atrophy, autosomal dominant: Undiagnosed Conditions

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Misdiagnosis and Optic atrophy, autosomal dominant

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis). See symptoms of Vitamin B12...read more »

Optic atrophy, autosomal dominant: Research Doctors & Specialists

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Optic atrophy, autosomal dominant: Animations

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Related Optic atrophy, autosomal dominant Info

More information about Optic atrophy, autosomal dominant

  1. Optic atrophy, autosomal dominant: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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