“…Widefield autofluorescence imaging, which is often used in most inherited retinal disease clinics, may detect presymptomatic retinitis pigmentosa and often demonstrates character-istic findings in carriers of X-linked disease, such as retinitis pigmentosa, choroideremia, or ocular albinism. 4 In some of these cases, retinal images can be so characteristic that they alone are often sufficient to diagnose carrier status, and hence, the familial inheritance pattern. Other examples include autosomal dominant disease, such as Sorsby fundus dystrophy, where latephase indocyanine green angiography may illustrate characteristic changes 5 or Stargardt-like disease where quantitative autofluorescence imaging may detect increased lipofuscin accumulation in absence of any other retinal changes.…”