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What is Nystagmus 2, congenital, autosomal dominant?

What is Nystagmus 2, congenital, autosomal dominant?

  • Nystagmus 2, congenital, autosomal dominant: A dominantly inherited eye disorder characterized by involuntary, rapid eye movement that occurs within the first three months of life. The eye tends to move horizontally and round and round in circles. The abnormal eye movement stems from a defect in the part of the brain that controls eye movement.

Nystagmus 2, congenital, autosomal dominant is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Nystagmus 2, congenital, autosomal dominant, or a subtype of Nystagmus 2, congenital, autosomal dominant, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Nystagmus 2, congenital, autosomal dominant: Introduction

Types of Nystagmus 2, congenital, autosomal dominant:

Broader types of Nystagmus 2, congenital, autosomal dominant:

What causes Nystagmus 2, congenital, autosomal dominant?

Causes of Nystagmus 2, congenital, autosomal dominant: see causes of Nystagmus 2, congenital, autosomal dominant

What are the symptoms of Nystagmus 2, congenital, autosomal dominant?

Symptoms of Nystagmus 2, congenital, autosomal dominant: see symptoms of Nystagmus 2, congenital, autosomal dominant

Nystagmus 2, congenital, autosomal dominant: Testing

Diagnostic testing: see tests for Nystagmus 2, congenital, autosomal dominant.

Misdiagnosis: see misdiagnosis and Nystagmus 2, congenital, autosomal dominant.

How is it treated?

Doctors and Medical Specialists for Nystagmus 2, congenital, autosomal dominant: Medical Geneticist ; see also doctors and medical specialists for Nystagmus 2, congenital, autosomal dominant.
Treatments for Nystagmus 2, congenital, autosomal dominant: see treatments for Nystagmus 2, congenital, autosomal dominant

Name and Aliases of Nystagmus 2, congenital, autosomal dominant

Main name of condition: Nystagmus 2, congenital, autosomal dominant

Other names or spellings for Nystagmus 2, congenital, autosomal dominant:

NYS2, nystagmus, congenital motor, 2

NYS2, Nystagmus congenital, motor 2
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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