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What is Cone-Rod Dystrophy 1?

What is Cone-Rod Dystrophy 1?

  • Cone-Rod Dystrophy 1: An inherited progressive eye disease involving deterioration of the cones and rods of the eye. The cone and rod cells make up the retina. Type 1 results from a genetic defect on chromosome 18q21.1-q21.3. Initially, visual acuity becomes impaired followed by loss of peripheral vision.

Cone-Rod Dystrophy 1: Introduction

Types of Cone-Rod Dystrophy 1:

Broader types of Cone-Rod Dystrophy 1:

How serious is Cone-Rod Dystrophy 1?

Prognosis of Cone-Rod Dystrophy 1: There is no cure for the condition and vision impairment tends to start early in life.

What causes Cone-Rod Dystrophy 1?

Causes of Cone-Rod Dystrophy 1: see causes of Cone-Rod Dystrophy 1

What are the symptoms of Cone-Rod Dystrophy 1?

Symptoms of Cone-Rod Dystrophy 1: see symptoms of Cone-Rod Dystrophy 1

Onset of Cone-Rod Dystrophy 1: childhood

Cone-Rod Dystrophy 1: Testing

Diagnostic testing: see tests for Cone-Rod Dystrophy 1.

Misdiagnosis: see misdiagnosis and Cone-Rod Dystrophy 1.

How is it treated?

Treatments for Cone-Rod Dystrophy 1: see treatments for Cone-Rod Dystrophy 1

Name and Aliases of Cone-Rod Dystrophy 1

Main name of condition: Cone-Rod Dystrophy 1

Other names or spellings for Cone-Rod Dystrophy 1:

CORD1

 

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