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Night blindness, congenital stationary

Night blindness, congenital stationary: Introduction

Night blindness, congenital stationary: A rare inherited disorder of the retina that involves the rods of the eyes. A reduced sharpness of vision and night blindness are usually the only symptoms. The disorder is non-progressive. More detailed information about the symptoms, causes, and treatments of Night blindness, congenital stationary is available below.

Symptoms of Night blindness, congenital stationary

Home Diagnostic Testing

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Wrongly Diagnosed with Night blindness, congenital stationary?

Causes of Night blindness, congenital stationary

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Night blindness, congenital stationary: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Night blindness, congenital stationary

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Night blindness, congenital stationary: Research Doctors & Specialists

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Hospitals & Clinics: Night blindness, congenital stationary

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Night blindness, congenital stationary: Animations

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Night blindness, congenital stationary: Broader Related Topics

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Definitions of Night blindness, congenital stationary:

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

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Night blindness, congenital stationary as a "rare disease".
Source - Orphanet

Related Night blindness, congenital stationary Info

More information about Night blindness, congenital stationary

  1. Night blindness, congenital stationary: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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