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Night blindness, congenital stationary, type 1B

Night blindness, congenital stationary, type 1B: Introduction

Night blindness, congenital stationary, type 1B: 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 non-progressive disorder is recessively inherited and is linked to a defect at chromosome 5q35. More detailed information about the symptoms, causes, and treatments of Night blindness, congenital stationary, type 1B is available below.

Symptoms of Night blindness, congenital stationary, type 1B

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Causes of Night blindness, congenital stationary, type 1B

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Night blindness, congenital stationary, type 1B: Undiagnosed Conditions

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Night blindness, congenital stationary, type 1B: Research Doctors & Specialists

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