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What is Retinitis Pigmentosa 7?

What is Retinitis Pigmentosa 7?

  • Retinitis Pigmentosa 7: 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 7 is linked to a genetic defect on chromosome 6p21.1.

Retinitis Pigmentosa 7: Introduction

Types of Retinitis Pigmentosa 7:

Broader types of Retinitis Pigmentosa 7:

How serious is Retinitis Pigmentosa 7?

Complications of Retinitis Pigmentosa 7: see complications of Retinitis Pigmentosa 7

What causes Retinitis Pigmentosa 7?

Causes of Retinitis Pigmentosa 7: see causes of Retinitis Pigmentosa 7
Cause of Retinitis Pigmentosa 7: The genetic anomaly is inherited in an autosomal dominant manner.

What are the symptoms of Retinitis Pigmentosa 7?

Symptoms of Retinitis Pigmentosa 7: see symptoms of Retinitis Pigmentosa 7

Complications of Retinitis Pigmentosa 7: see complications of Retinitis Pigmentosa 7

Retinitis Pigmentosa 7: Testing

Diagnostic testing: see tests for Retinitis Pigmentosa 7.

Misdiagnosis: see misdiagnosis and Retinitis Pigmentosa 7.

How is it treated?

Treatments for Retinitis Pigmentosa 7: see treatments for Retinitis Pigmentosa 7

Name and Aliases of Retinitis Pigmentosa 7

Main name of condition: Retinitis Pigmentosa 7

Other names or spellings for Retinitis Pigmentosa 7:

RP7

 

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