AF in Myriad Retinal Degenerations-Part 2 – Page 42 of 62
Case 9: Optomap® FAF Image OD Note the “monotonous” hyper-AF dots suggesting that this condition may not be completely stationary as written about by others.
Case 9: Optomap® FAF Image OD Note the “monotonous” hyper-AF dots suggesting that this condition may not be completely stationary as written about by others.
Case 9: Optomap® Color Fundus Image OD Case 9: A 10 yo AM presented with numerous, subtle, uniform, dot lesions throughout the posterior pole in both eyes. The patient reported no visual problems and his mother did not note any activity consistent with visual deficits. BCVA was 20/30 in both eyes. SD OCT
Case 8: Optomap® Color Fundus and AF Comparison OD and OS KEY: Color Optomap Auto Fluorescence This is a case of pericentral RP which has some asymmetries. Visual fields of this case are predictable from the AF images and are available at #RR 52 page 7
Case 8: Optomap®FAF Image OD The left eye reveals a bulls eye maculopathy that was not really visualized in the RE.
Case 8: Optomap® Color Fundus Image OS Note somewhat simIlar findings in the left eye.
Case 8: Optomap® FAF Image OD Note the large zone of hyper-AF, suggesting further progression of RPE loss in these areas.
Case 8: Optomap® Color Fundus Image OD Case 8: A 47 yo BM presented with progressive difficulties with both day and night vision. His symptoms began about a decade earlier. BCVA was 20/60 OD and 20/70-OS. Pigmentary changes were noted inferior to the inferior arcades with slight arterial attenuation inferiorly in the right
Case 7: Optomap® Color Fundus and AF Comparison OD and OS KEY: Color Optomap Auto Fluorescence Based upon the asymmetric hyper AF patterns, eventual vision loss is more likely in the left eye than in the right.
Case 7: Optomap® FAF Image OS The drusen appear to hyper-AF in this case and some small zones of hypo-AF are also visible. Careful follow-up is warranted.
Case 7: Optomap® Color Fundus Image OS Somewhat similar drusen deposits are noted in the macula of the LE.