Optical Coherence Tomography in Inherited Macular Dystrophies: A Review

Author:

Gómez-Benlloch Alba12,Garrell-Salat Xavier12,Cobos Estefanía3,López Elena1,Esteve-Garcia Anna4,Ruiz Sergi1,Vázquez Meritxell1,Sararols Laura12,Biarnés Marc1ORCID

Affiliation:

1. Oftalmologia Mèdica i Quirúrgica (OMIQ) Research, c/Tamarit 39, 08205 Sabadell, Spain

2. Department of Ophthalmology, Hospital General de Granollers, Av Francesc Ribas s/n, 08402 Granollers, Spain

3. Hospital Universitari de Bellvitge, c/De la Feixa Llarga s/n, 08907 L’Hospitalet de Llobregat, Spain

4. Clinical Genetics Unit, Laboratori Clinic Territorial Metropolitada Sud, Hospital Universitari de Bellvitge, Institut d’Investigació Biomèdica de Bellvitge (IDIBELL), c/De la Feixa Llarga s/n, 08907 L’Hospitalet de Llobregat, Spain

Abstract

Macular dystrophies (MDs) constitute a collection of hereditary retina disorders leading to notable visual impairment, primarily due to progressive macular atrophy. These conditions are distinguished by bilateral and relatively symmetrical abnormalities in the macula that significantly impair central visual function. Recent strides in fundus imaging, especially optical coherence tomography (OCT), have enhanced our comprehension and diagnostic capabilities for MD. OCT enables the identification of neurosensory retinal disorganization patterns and the extent of damage to retinal pigment epithelium (RPE) and photoreceptor cells in the dystrophies before visible macular pathology appears on fundus examinations. It not only helps us in diagnostic retinal and choroidal pathologies but also guides us in monitoring the progression of, staging of, and response to treatment. In this review, we summarize the key findings on OCT in some of the most common MD.

Publisher

MDPI AG

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