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
See full list of 8
symptoms of Cone-Rod Dystrophy 13
Home Diagnostic Testing
Home medical testing related to Cone-Rod Dystrophy 13:
- Vision & Eye Health: Home Testing:
- more...»
Wrongly Diagnosed with Cone-Rod Dystrophy 13?
Causes of Cone-Rod Dystrophy 13
- The condition is inherited in an autosomal recessive manner
- more causes...»
Read more about 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:
Other doctor, physician and specialist research services:
Cone-Rod Dystrophy 13: Animations
More Cone-Rod Dystrophy 13 animations & videos
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.
More about prognosis of Cone-Rod Dystrophy 13
Cone-Rod Dystrophy 13: Broader Related Topics
Types of Cone-Rod Dystrophy 13
User Interactive Forums
Read about other experiences, ask a question about Cone-Rod Dystrophy 13, or answer someone else's question, on our message boards:
Contents for Cone-Rod Dystrophy 13: