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Amaurosis congenita of Leber, type 10

Amaurosis congenita of Leber, type 10: Introduction

Amaurosis congenita of Leber, type 10: A rare inherited retinal disease (retinal dystrophy) that starts during the fetal stage. Vision impairment is obvious at birth or within months of birth. Type 10 is distinguished from the other forms of this condition by the genetic origin of the defect - chromosome 12, CEP290 gene. More detailed information about the symptoms, causes, and treatments of Amaurosis congenita of Leber, type 10 is available below.

Symptoms of Amaurosis congenita of Leber, type 10

Home Diagnostic Testing

Home medical testing related to Amaurosis congenita of Leber, type 10:

Wrongly Diagnosed with Amaurosis congenita of Leber, type 10?

Causes of Amaurosis congenita of Leber, type 10

Read more about causes of Amaurosis congenita of Leber, type 10.

Amaurosis congenita of Leber, type 10: Undiagnosed Conditions

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Amaurosis congenita of Leber, type 10: Research Doctors & Specialists

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Amaurosis congenita of Leber, type 10: Animations

Amaurosis congenita of Leber, type 10: Broader Related Topics

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Related Amaurosis congenita of Leber, type 10 Info

More information about Amaurosis congenita of Leber, type 10

  1. Amaurosis congenita of Leber, type 10: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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