Titlebook: Atlas of Fundus Autofluorescence Imaging; Frank Holz,Richard Spaide,Steffen Schmitz-Valckenb Book 2007 Springer-Verlag Berlin Heidelberg 2

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Autofluorescence Imaging with the Fundus Camerasosomes and eventually become lipofuscin. Since the accumulation of lipofuscin occurs in RPE cells because of their unique metabolic role [1–3], autofluorescence imaging provides functional information about these cells.

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Macular Pigment Measurement —Clinical Applicationse based on fundus imaging, focused solely on the peak optical density at the fovea and ignored the lateral distribution [3, 4, 21, 22]. A possible role for MP in the pathophysiology of age-related macular degeneration (AMD) has been suggested [2, 5], and Trieschmann et al. have reported that this can be related to the MP profiles [19].

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Discrete Lines of Increased Fundus Autofluorescence in Various Forms of Retinal Dystrophiesor cone-rod dystrophy (CRD)—the similar appearance on FAF images and the concordance of functional findings indicate that these lines in heterogeneous diseases entities share a common underlying pathophysiologic mechanism.

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Chorioretinal Inflammatory Disordersdisease. However, autofluorescence photography is almost always used with alternate means of imaging, such as optical coherence tomography (OCT), fluorescein angiography, and indocyanine green (ICG) angiography. Autofluorescence photography contributes information that alternate methods of imaging cannot and does so through a noninvasive means.

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