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Night blindness, congenital stationary, autosomal dominant

Night blindness, congenital stationary, autosomal dominant: Introduction

Night blindness, congenital stationary, autosomal dominant: 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 dominantly inherited. More detailed information about the symptoms, causes, and treatments of Night blindness, congenital stationary, autosomal dominant is available below.

Symptoms of Night blindness, congenital stationary, autosomal dominant

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Night blindness, congenital stationary, autosomal dominant: Related Patient Stories

Causes of Night blindness, congenital stationary, autosomal dominant

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Night blindness, congenital stationary, autosomal dominant: Undiagnosed Conditions

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Misdiagnosis and Night blindness, congenital stationary, autosomal dominant

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