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What is Retinal cone dystrophy 3A?

What is Retinal cone dystrophy 3A?

  • 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.

Retinal cone dystrophy 3A: Introduction

Types of Retinal cone dystrophy 3A:

Broader types of Retinal cone dystrophy 3A:

What causes Retinal cone dystrophy 3A?

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

What are the symptoms of Retinal cone dystrophy 3A?

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

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

Retinal cone dystrophy 3A: Testing

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

Misdiagnosis: see misdiagnosis and Retinal cone dystrophy 3A.

How is it treated?

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

Name and Aliases of Retinal cone dystrophy 3A

Main name of condition: Retinal cone dystrophy 3A

Other names or spellings for Retinal cone dystrophy 3A:

Cone Dystrophy with Night Blindness and Supernormal Rod Responses, PDE6H-related, RCD3A

 

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