Night blindness, congenital stationary, type 2B: 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 11q13.1. More detailed information about the symptoms, causes, and treatments of Night blindness, congenital stationary, type 2B is available below.
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