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Retinal cone dystrophy 3A

Retinal cone dystrophy 3A: Introduction

Retinal cone dystrophy 3A: An inherited eye disease characterized by the deterioration of the retinal cones. Type 3A is linked to a defect on chromosome 12p13. More detailed information about the symptoms, causes, and treatments of Retinal cone dystrophy 3A is available below.

Symptoms of Retinal cone dystrophy 3A

Home Diagnostic Testing

Home medical testing related to Retinal cone dystrophy 3A:

Wrongly Diagnosed with Retinal cone dystrophy 3A?

Causes of Retinal cone dystrophy 3A

  • The genetic condition is inherited in an autosomal dominant manner
  • more causes...»

More information about causes of Retinal cone dystrophy 3A:

Retinal cone dystrophy 3A: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Retinal cone dystrophy 3A: Research Doctors & Specialists

Research related physicians and medical specialists:

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Retinal cone dystrophy 3A: Animations

Retinal cone dystrophy 3A: Broader Related Topics

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Related Retinal cone dystrophy 3A Info

More information about Retinal cone dystrophy 3A

  1. Retinal cone dystrophy 3A: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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