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Retinal cone dystrophy 2

Retinal cone dystrophy 2: Introduction

Retinal cone dystrophy 2: An inherited eye disease characterized by the deterioration of the retinal cones. Vision loss tends to start during the first decade of life and slowly progresses into adulthood. Type 2 is linked to a defect on chromosome 17p. More detailed information about the symptoms, causes, and treatments of Retinal cone dystrophy 2 is available below.

Symptoms of Retinal cone dystrophy 2

Home Diagnostic Testing

Home medical testing related to Retinal cone dystrophy 2:

Wrongly Diagnosed with Retinal cone dystrophy 2?

Causes of Retinal cone dystrophy 2

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

More information about causes of Retinal cone dystrophy 2:

Retinal cone dystrophy 2: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Retinal cone dystrophy 2: Research Doctors & Specialists

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Retinal cone dystrophy 2: Animations

Retinal cone dystrophy 2: Broader Related Topics

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Related Retinal cone dystrophy 2 Info

More information about Retinal cone dystrophy 2

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

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