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Amaurosis congenita of Leber

Amaurosis congenita of Leber: Introduction

Amaurosis congenita of Leber: A rare genetic eye disorder characterized by blindness at birth or within years as well as other eye abnormalities. More detailed information about the symptoms, causes, and treatments of Amaurosis congenita of Leber is available below.

Symptoms of Amaurosis congenita of Leber

Home Diagnostic Testing

Home medical testing related to Amaurosis congenita of Leber:

Wrongly Diagnosed with Amaurosis congenita of Leber?

Amaurosis congenita of Leber: Related Patient Stories

Causes of Amaurosis congenita of Leber

Read more about causes of Amaurosis congenita of Leber.

Disease Topics Related To Amaurosis congenita of Leber

Research the causes of these diseases that are similar to, or related to, Amaurosis congenita of Leber:

Less Common Symptoms of Amaurosis congenita of Leber

Amaurosis congenita of Leber: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Amaurosis congenita of Leber: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Amaurosis congenita of Leber: Animations

Statistics for Amaurosis congenita of Leber

Amaurosis congenita of Leber: Broader Related Topics

User Interactive Forums

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Definitions of Amaurosis congenita of Leber:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Amaurosis congenita of Leber as a "rare disease".
Source - Orphanet

 

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