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What is Amaurosis Congenita of Leber, type 12?

What is Amaurosis Congenita of Leber, type 12?

  • Amaurosis Congenita of Leber, type 12: A rare inherited retinal disease (retinal dystrophy) that usually starts during the fetal stage. Vision impairment is usually apparent at birth or within months of birth. Type 12 is distinguished from the other forms of this condition by the genetic origin of the defect - chromosome 1q32.3.

Amaurosis Congenita of Leber, type 12: Introduction

Types of Amaurosis Congenita of Leber, type 12:

Broader types of Amaurosis Congenita of Leber, type 12:

What causes Amaurosis Congenita of Leber, type 12?

Causes of Amaurosis Congenita of Leber, type 12: see causes of Amaurosis Congenita of Leber, type 12

What are the symptoms of Amaurosis Congenita of Leber, type 12?

Symptoms of Amaurosis Congenita of Leber, type 12: see symptoms of Amaurosis Congenita of Leber, type 12

Amaurosis Congenita of Leber, type 12: Testing

Diagnostic testing: see tests for Amaurosis Congenita of Leber, type 12.

Misdiagnosis: see misdiagnosis and Amaurosis Congenita of Leber, type 12.

How is it treated?

Treatments for Amaurosis Congenita of Leber, type 12: see treatments for Amaurosis Congenita of Leber, type 12

Name and Aliases of Amaurosis Congenita of Leber, type 12

Main name of condition: Amaurosis Congenita of Leber, type 12

Other names or spellings for Amaurosis Congenita of Leber, type 12:

LCA12

 

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