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What is Retinitis Pigmentosa 35?

What is Retinitis Pigmentosa 35?

  • Retinitis Pigmentosa 35: 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 35 is linked to a genetic defect on chromosome 1q22.

Retinitis Pigmentosa 35: Introduction

Types of Retinitis Pigmentosa 35:

Broader types of Retinitis Pigmentosa 35:

How serious is Retinitis Pigmentosa 35?

Complications of Retinitis Pigmentosa 35: see complications of Retinitis Pigmentosa 35

What causes Retinitis Pigmentosa 35?

Causes of Retinitis Pigmentosa 35: see causes of Retinitis Pigmentosa 35
Cause of Retinitis Pigmentosa 35: The genetic anomaly is inherited in an autosomal recessive or dominant manner.

What are the symptoms of Retinitis Pigmentosa 35?

Symptoms of Retinitis Pigmentosa 35: see symptoms of Retinitis Pigmentosa 35

Complications of Retinitis Pigmentosa 35: see complications of Retinitis Pigmentosa 35

Retinitis Pigmentosa 35: Testing

Diagnostic testing: see tests for Retinitis Pigmentosa 35.

Misdiagnosis: see misdiagnosis and Retinitis Pigmentosa 35.

How is it treated?

Treatments for Retinitis Pigmentosa 35: see treatments for Retinitis Pigmentosa 35

Name and Aliases of Retinitis Pigmentosa 35

Main name of condition: Retinitis Pigmentosa 35

Other names or spellings for Retinitis Pigmentosa 35:

RP35

 

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