MaculaTo determine if eyes with the foveal crack sign (FCS) in macular pattern dystrophy (MPD) progress to macular holes, and if FCS occurs in the context of hyperreflective foci (HRF) that do not reach the threshold of FCS.: A retrospective chart review of eyes with MPD was conducted ...
We present a case of reticular pattern dystrophy of the retinal pigment epithelium (RPE) in a 64-year-old woman. Fundus examination revealed discoloration at the macula in both eyes. Fundus autofluorescence (FAF) imaging showed clearly defined reticular hyperfluorescent lesions. Optical coherence ...
However, exclusion of possible genetic defects would further support the conclusion of an acquired pattern dystrophy of the macula induced by desferrioxamine. Adjustment of chelation treatment could have been a more proactive approach. However, in our cases, haematologist consultation suggested that ...
Macula OCT showed focal atrophic regions bilaterally corresponding to hypoautofluorescence areas on FAF. ISCEV standards PVEPs, PERG and FFERG were normal. mERG responses corresponding to the atrophic areas on OCT were reduced. These findings were compatible with pattern dystrophy. Genetic testing was...
Conclusions : Rod and cone sensitivity was decreased in subjects with the P210R mutation in PRPH2. However absolute vision loss occurred within the macula and likely secondary to drusen formation. This suggests that although rod and cone photoreceptors are dependent on PRPH2, preventing blindness ...
Common spectral domain OCT and electrophysiological findings in different pattern dystrophiesDystrophyMaculaObjectives (1) To investigate and integrate the tomographic, angiographic and electrodiagnostic findings in pattern dystrophy. (2) To correlate visual acuity (VA) with central macular thickness (CMT),...