Vitreo-macular interface disorders in retinitis pigmentosa.

Serena FragiottaTommaso RossiCarmela CarnevaleAlessandro CutiniStefano TricaricoLorenzo CasilloGianluca ScuderiEnzo Maria Vingolo

Published in: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie (2019)

Our study confirms the high prevalence of VMID in RP patients; however, only ERMs determined a significant loss of vision over 24 months. The high prevalence of VMID in RP patients suggests that macular alteration other than edema represents part of disease spectrum.

Keyphrases

end stage renal disease
ejection fraction
newly diagnosed
prognostic factors
peritoneal dialysis
optical coherence tomography