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Retinitis Pigmentosa 37

Retinitis Pigmentosa 37: Introduction

Retinitis Pigmentosa 37: 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 37 is linked to a genetic defect on chromosome 15q23. More detailed information about the symptoms, causes, and treatments of Retinitis Pigmentosa 37 is available below.

Symptoms of Retinitis Pigmentosa 37

Treatments for Retinitis Pigmentosa 37

  • 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...»

Home Diagnostic Testing

Home medical testing related to Retinitis Pigmentosa 37:

Wrongly Diagnosed with Retinitis Pigmentosa 37?

Retinitis Pigmentosa 37: Complications

Review possible medical complications related to Retinitis Pigmentosa 37:

Causes of Retinitis Pigmentosa 37

Read more about causes of Retinitis Pigmentosa 37.

Retinitis Pigmentosa 37: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Retinitis Pigmentosa 37

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Retinitis Pigmentosa 37: Research Doctors & Specialists

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Retinitis Pigmentosa 37: Animations

Retinitis Pigmentosa 37: Broader Related Topics

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Related Retinitis Pigmentosa 37 Info

More information about Retinitis Pigmentosa 37

  1. Retinitis Pigmentosa 37: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications

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