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What is Retinal cone dystrophy 1?

What is Retinal cone dystrophy 1?

  • Retinal cone dystrophy 1: An inherited eye disease characterized by the deterioration of the retinal cones. Loss of visual acuity tends to start in the third decade of life. Type 1 is linked to a defect on chromosome 6q25-q26.

Retinal cone dystrophy 1: Introduction

Types of Retinal cone dystrophy 1:

Broader types of Retinal cone dystrophy 1:

What causes Retinal cone dystrophy 1?

Causes of Retinal cone dystrophy 1: see causes of Retinal cone dystrophy 1

What are the symptoms of Retinal cone dystrophy 1?

Symptoms of Retinal cone dystrophy 1: see symptoms of Retinal cone dystrophy 1

Onset of Retinal cone dystrophy 1: Usually during the third decade of life or later.

Retinal cone dystrophy 1: Testing

Diagnostic testing: see tests for Retinal cone dystrophy 1.

Misdiagnosis: see misdiagnosis and Retinal cone dystrophy 1.

How is it treated?

Treatments for Retinal cone dystrophy 1: see treatments for Retinal cone dystrophy 1

Name and Aliases of Retinal cone dystrophy 1

Main name of condition: Retinal cone dystrophy 1

Other names or spellings for Retinal cone dystrophy 1:

Cone Degeneration, autosomal dominant, RCD1

 

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