Retinitis Pigmentosa 22
Retinitis Pigmentosa 22: Introduction
Retinitis Pigmentosa 22: Retinitis pigmentosa is an inherited eye disorder characterized by progressive loss of peripheral vision and night vision difficulties that can cause central vision loss. There are a large number of genes linked to retinitis pigmentosa. Type 22 is linked to a genetic defect on chromosome 16p12.3-p12.1.
More detailed information about the symptoms,
causes, and treatments of Retinitis Pigmentosa 22 is available below.
Symptoms of Retinitis Pigmentosa 22
See full list of 8
symptoms of Retinitis Pigmentosa 22
Treatments for Retinitis Pigmentosa 22
- There is no cure for the condition but complete loss of vision is considered uncommon for the disease
- It is recommended that sunglasses be worn regularly to protect them from UV light
- Regular screening should be undertaken to monitor for such things as cataracts
- Research is still evaluating the benefits of vitamin A and DHA in slowing the progression of the condition
- Low vision aids will help a person function better on a day to day basis e.g. electronic, optical, mechanical and computer-based aids
- more treatments...»
See full list of 6
treatments for Retinitis Pigmentosa 22
Home Diagnostic Testing
Home medical testing related to Retinitis Pigmentosa 22:
- Vision & Eye Health: Home Testing:
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Wrongly Diagnosed with Retinitis Pigmentosa 22?
Retinitis Pigmentosa 22: Complications
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Causes of Retinitis Pigmentosa 22
Read more about causes of Retinitis Pigmentosa 22.
Retinitis Pigmentosa 22: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and Retinitis Pigmentosa 22
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Retinitis Pigmentosa 22: Research Doctors & Specialists
Research related physicians and medical specialists:
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Retinitis Pigmentosa 22: Animations
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Retinitis Pigmentosa 22: Broader Related Topics
Types of Retinitis Pigmentosa 22
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