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Retinal cone dystrophy 3B

Retinal cone dystrophy 3B: Introduction

Retinal cone dystrophy 3B: An inherited eye disease characterized by the deterioration of the retinal cones. Type 3B is linked to a defect on the PKCNV2 gene. More detailed information about the symptoms, causes, and treatments of Retinal cone dystrophy 3B is available below.

Symptoms of Retinal cone dystrophy 3B

Home Diagnostic Testing

Home medical testing related to Retinal cone dystrophy 3B:

Wrongly Diagnosed with Retinal cone dystrophy 3B?

Causes of Retinal cone dystrophy 3B

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

More information about causes of Retinal cone dystrophy 3B:

Retinal cone dystrophy 3B: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Retinal cone dystrophy 3B: Research Doctors & Specialists

Research related physicians and medical specialists:

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Retinal cone dystrophy 3B: Animations

Retinal cone dystrophy 3B: Broader Related Topics

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Related Retinal cone dystrophy 3B Info

More information about Retinal cone dystrophy 3B

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

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