Vitreo-macular interface disorders in retinitis pigmentosa.
Serena FragiottaTommaso RossiCarmela CarnevaleAlessandro CutiniStefano TricaricoLorenzo CasilloGianluca ScuderiEnzo Maria VingoloPublished 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.