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What is Retinitis Pigmentosa 49?

What is Retinitis Pigmentosa 49?

  • Retinitis Pigmentosa 49: 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 49 is linked to a genetic defect on chromosome 4p12-cen.

Retinitis Pigmentosa 49: Introduction

Types of Retinitis Pigmentosa 49:

Broader types of Retinitis Pigmentosa 49:

How serious is Retinitis Pigmentosa 49?

Complications of Retinitis Pigmentosa 49: see complications of Retinitis Pigmentosa 49

What causes Retinitis Pigmentosa 49?

Causes of Retinitis Pigmentosa 49: see causes of Retinitis Pigmentosa 49
Cause of Retinitis Pigmentosa 49: The genetic anomaly is inherited in an autosomal recessive manner.

What are the symptoms of Retinitis Pigmentosa 49?

Symptoms of Retinitis Pigmentosa 49: see symptoms of Retinitis Pigmentosa 49

Complications of Retinitis Pigmentosa 49: see complications of Retinitis Pigmentosa 49

Retinitis Pigmentosa 49: Testing

Diagnostic testing: see tests for Retinitis Pigmentosa 49.

Misdiagnosis: see misdiagnosis and Retinitis Pigmentosa 49.

How is it treated?

Treatments for Retinitis Pigmentosa 49: see treatments for Retinitis Pigmentosa 49

Name and Aliases of Retinitis Pigmentosa 49

Main name of condition: Retinitis Pigmentosa 49

Other names or spellings for Retinitis Pigmentosa 49:

RP490

 

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