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What is Amaurosis congenita of Leber, type 10?

What is Amaurosis congenita of Leber, type 10?

  • 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.

Amaurosis congenita of Leber, type 10: Introduction

Types of Amaurosis congenita of Leber, type 10:

Broader types of Amaurosis congenita of Leber, type 10:

What causes Amaurosis congenita of Leber, type 10?

Causes of Amaurosis congenita of Leber, type 10: see causes of Amaurosis congenita of Leber, type 10

What are the symptoms of Amaurosis congenita of Leber, type 10?

Symptoms of Amaurosis congenita of Leber, type 10: see symptoms of Amaurosis congenita of Leber, type 10

Amaurosis congenita of Leber, type 10: Testing

Diagnostic testing: see tests for Amaurosis congenita of Leber, type 10.

Misdiagnosis: see misdiagnosis and Amaurosis congenita of Leber, type 10.

How is it treated?

Doctors and Medical Specialists for Amaurosis congenita of Leber, type 10: Medical Geneticist ; see also doctors and medical specialists for Amaurosis congenita of Leber, type 10.
Treatments for Amaurosis congenita of Leber, type 10: see treatments for Amaurosis congenita of Leber, type 10

Name and Aliases of Amaurosis congenita of Leber, type 10

Main name of condition: Amaurosis congenita of Leber, type 10

Other names or spellings for Amaurosis congenita of Leber, type 10:

LCA10, Leber congenital amaurosis, type X, Amaurosis congenita of Leber, type X

 

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