Retinitis Pigmentosa 2

Retinitis Pigmentosa 2:

Retinitis Pigmentosa 2: Introduction

Retinitis Pigmentosa 2: 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 2 is linked to a genetic defect on chromosome Xp11.3. More detailed information about the symptoms, causes, and treatments of Retinitis Pigmentosa 2 is available below.

Symptoms of Retinitis Pigmentosa 2

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See full list of 8 symptoms of Retinitis Pigmentosa 2

Treatments for Retinitis Pigmentosa 2

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
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See full list of 6 treatments for Retinitis Pigmentosa 2

Home Diagnostic Testing

Home medical testing related to Retinitis Pigmentosa 2:

Vision & Eye Health: Home Testing:
- Home Eye Tests
- Home Vision Tests
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Wrongly Diagnosed with Retinitis Pigmentosa 2?

Retinitis Pigmentosa 2: Complications

Review possible medical complications related to Retinitis Pigmentosa 2:

Retinal damage (see Retina symptoms)
Retinal swelling (see Retina symptoms)
Blindness
Cataracts - patients tend to be more prone to the early development of cataracts
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Causes of Retinitis Pigmentosa 2

Read more about causes of Retinitis Pigmentosa 2.

Retinitis Pigmentosa 2: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Vision & Eye: serious diseases often undiagnosed:
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Misdiagnosis and Retinitis Pigmentosa 2

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