Stargardt disease: Multimodal imaging: A review

Research output: Contribution to journalReview articlepeer-review

6 Citations (Scopus)

Abstract

Stargardt disease (STGD1) is an autosomal recessive retinal dystrophy, characterised by bilateral progressive central vision loss and subretinal deposition of lipofuscin-like substances. Recent advances in molecular diagnosis and therapeutic options are complemented by the increasing recognition of new multimodal imaging biomarkers that may predict genotype and disease progression. Unique non-invasive imaging features of STDG1 are useful for gene variant interpretation and may even provide insight into the underlying molecular pathophysiology. In addition, pathognomonic imaging features of STGD1 have been used to train neural networks to improve time efficiency in lesion segmentation and disease progression measurements. This review will discuss the role of key imaging modalities, correlate imaging signs across varied STGD1 presentations and illustrate the use of multimodal imaging as an outcome measure in determining the efficacy of emerging STGD1 specific therapies.

Original languageEnglish
Pages (from-to)498-515
Number of pages18
JournalClinical and Experimental Ophthalmology
Volume49
Issue number5
DOIs
Publication statusPublished - Jul 2021

Fingerprint

Dive into the research topics of 'Stargardt disease: Multimodal imaging: A review'. Together they form a unique fingerprint.

Cite this