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Cone-Rod Dystrophy 13

Cone-Rod Dystrophy 13: Introduction

Cone-Rod Dystrophy 13: 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 13 results from a genetic defect on chromosome 14q11. Initially, visual acuity becomes impaired followed by loss of peripheral vision. More detailed information about the symptoms, causes, and treatments of Cone-Rod Dystrophy 13 is available below.

Symptoms of Cone-Rod Dystrophy 13

Home Diagnostic Testing

Home medical testing related to Cone-Rod Dystrophy 13:

Wrongly Diagnosed with Cone-Rod Dystrophy 13?

Causes of Cone-Rod Dystrophy 13

More information about causes of Cone-Rod Dystrophy 13:

Cone-Rod Dystrophy 13: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Cone-Rod Dystrophy 13: Research Doctors & Specialists

Research related physicians and medical specialists:

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Cone-Rod Dystrophy 13: Animations

Prognosis for Cone-Rod Dystrophy 13

Prognosis for Cone-Rod Dystrophy 13: There is no cure for the condition and vision impairment tends to start early in life.

Cone-Rod Dystrophy 13: Broader Related Topics

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Related Cone-Rod Dystrophy 13 Info

More information about Cone-Rod Dystrophy 13

  1. Cone-Rod Dystrophy 13: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Prognosis
 

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