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Nystagmus 2, congenital, autosomal dominant

Nystagmus 2, congenital, autosomal dominant: Introduction

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. More detailed information about the symptoms, causes, and treatments of Nystagmus 2, congenital, autosomal dominant is available below.

Symptoms of Nystagmus 2, congenital, autosomal dominant

Home Diagnostic Testing

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Causes of Nystagmus 2, congenital, autosomal dominant

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Nystagmus 2, congenital, autosomal dominant: Undiagnosed Conditions

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Misdiagnosis and Nystagmus 2, congenital, autosomal dominant

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Nystagmus 2, congenital, autosomal dominant: Research Doctors & Specialists

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Nystagmus 2, congenital, autosomal dominant: Animations

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Definitions of Nystagmus 2, congenital, autosomal dominant:

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)

Related Nystagmus 2, congenital, autosomal dominant Info

More information about Nystagmus 2, congenital, autosomal dominant

  1. Nystagmus 2, congenital, autosomal dominant: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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