Inability to see well at night or in poor light.

Diminished clarity of vision.

A pale yellow discoloration of the optic disc (the area of the optic nerve head in the retina). The optic disc normally has a pinkish hue with a central yellowish depression.

Progressive maculopathy characterized by concentric regions of hyper- and hypo-pigmentation.

Pigment migration into the retina in a bone-spicule configuration (resembling the nucleated cells within the lacuna of bone).

An absolute or relative reduction in the extent of the normal field of vision.

An inherited retinal disease subtype in which the rod photoreceptors appear to be more severely affected than the cone photoreceptors. Typical presentation is with nyctalopia (due to rod dysfunction) followed by loss of mid-peripheral field of vision, which gradually extends and leaves many patients with a small central island of vision due to the preservation of macular cones.