Inherited retinal dystrophies and cone dysfunction syndromes may show a sharp hyporeflective interruption in the outermost retinal layers on optical coherence tomography (OCT), known as foveal cavitation (FC). The aim of the study was to describe the morpho-functional features of FC in patients affected by retinal dystrophies by means of multimodal imaging.
Multimodal imaging of foveal cavitation in retinal dystrophies / Parodi, Maurizio Battaglia; Cicinelli, Maria Vittoria; Iacono, Pierluigi; Bolognesi, Gianluigi; Bandello, Francesco. - In: GRAEFE'S ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY. - ISSN 0721-832X. - 255:2(2017), pp. 271-279-279. [10.1007/s00417-016-3450-7]
Multimodal imaging of foveal cavitation in retinal dystrophies
Parodi, Maurizio Battaglia;Cicinelli, Maria Vittoria;Bandello, Francesco
2017-01-01
Abstract
Inherited retinal dystrophies and cone dysfunction syndromes may show a sharp hyporeflective interruption in the outermost retinal layers on optical coherence tomography (OCT), known as foveal cavitation (FC). The aim of the study was to describe the morpho-functional features of FC in patients affected by retinal dystrophies by means of multimodal imaging.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
