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What is Amaurosis congenita of Leber, type 6?

What is Amaurosis congenita of Leber, type 6?

  • Amaurosis congenita of Leber, type 6: 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 6 is distinguished from the other forms of this condition by the genetic origin of the defect - chromosome 14q11, RPGRIP1 gene.

Amaurosis congenita of Leber, type 6: Introduction

Types of Amaurosis congenita of Leber, type 6:

Broader types of Amaurosis congenita of Leber, type 6:

What causes Amaurosis congenita of Leber, type 6?

Causes of Amaurosis congenita of Leber, type 6: see causes of Amaurosis congenita of Leber, type 6

What are the symptoms of Amaurosis congenita of Leber, type 6?

Symptoms of Amaurosis congenita of Leber, type 6: see symptoms of Amaurosis congenita of Leber, type 6

Amaurosis congenita of Leber, type 6: Testing

Diagnostic testing: see tests for Amaurosis congenita of Leber, type 6.

Misdiagnosis: see misdiagnosis and Amaurosis congenita of Leber, type 6.

How is it treated?

Doctors and Medical Specialists for Amaurosis congenita of Leber, type 6: Medical Geneticist ; see also doctors and medical specialists for Amaurosis congenita of Leber, type 6.
Treatments for Amaurosis congenita of Leber, type 6: see treatments for Amaurosis congenita of Leber, type 6

Name and Aliases of Amaurosis congenita of Leber, type 6

Main name of condition: Amaurosis congenita of Leber, type 6

Other names or spellings for Amaurosis congenita of Leber, type 6:

LCA6, Leber congenital amaurosis, type 6, Amaurosis congenita of Leber, type VU, Leber congenital amaurosis, type VI

Amaurosis congenita of Leber, type 6: Related Conditions

Research the causes of these diseases that are similar to, or related to, Amaurosis congenita of Leber, type 6:

 

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