Retinal cone dystrophy 2
Retinal cone dystrophy 2: Introduction
Retinal cone dystrophy 2: An inherited eye disease characterized by the deterioration of the retinal cones. Vision loss tends to start during the first decade of life and slowly progresses into adulthood. Type 2 is linked to a defect on chromosome 17p.
More detailed information about the symptoms,
causes, and treatments of Retinal cone dystrophy 2 is available below.
Symptoms of Retinal cone dystrophy 2
See full list of 7
symptoms of Retinal cone dystrophy 2
Home Diagnostic Testing
Home medical testing related to Retinal cone dystrophy 2:
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Wrongly Diagnosed with Retinal cone dystrophy 2?
Causes of Retinal cone dystrophy 2
- The genetic condition is inherited in an autosomal dominant manner
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Retinal cone dystrophy 2: Undiagnosed Conditions
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Retinal cone dystrophy 2: Research Doctors & Specialists
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Retinal cone dystrophy 2: Animations
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Retinal cone dystrophy 2: Broader Related Topics
Types of Retinal cone dystrophy 2
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