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What is Retinal cone dystrophy 3B?

What is Retinal cone dystrophy 3B?

  • 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.

Retinal cone dystrophy 3B: Introduction

Types of Retinal cone dystrophy 3B:

Broader types of Retinal cone dystrophy 3B:

What causes Retinal cone dystrophy 3B?

Causes of Retinal cone dystrophy 3B: see causes of Retinal cone dystrophy 3B

What are the symptoms of Retinal cone dystrophy 3B?

Symptoms of Retinal cone dystrophy 3B: see symptoms of Retinal cone dystrophy 3B

Onset of Retinal cone dystrophy 3B: Usually during the first ten years of life.

Retinal cone dystrophy 3B: Testing

Diagnostic testing: see tests for Retinal cone dystrophy 3B.

Misdiagnosis: see misdiagnosis and Retinal cone dystrophy 3B.

How is it treated?

Treatments for Retinal cone dystrophy 3B: see treatments for Retinal cone dystrophy 3B

Name and Aliases of Retinal cone dystrophy 3B

Main name of condition: Retinal cone dystrophy 3B

Other names or spellings for Retinal cone dystrophy 3B:

Cone Dystrophy with Night Blindness and Supernormal Rod Responses, PKCNV2-related, RCD3B

 

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