Characterisation of microvascular abnormalities using OCT angiography in patients with biallelic variants in USH2A and MYO7A.

Ahmed M HagagAndreas MitsiosJasdeep Singh GillJoan M Nunez Do RioVasileios TheofylaktopoulosSarah HoustonAndrew R WebsterAdam M DubisMariya Moosajee

Published in: The British journal of ophthalmology (2019)

OCTA was able to detect similar retinal microvascular changes in patients with USH2A and MYO7A mutations. The CC was generally affected in MYO7A mutations. OCT angiography may further enhance our understanding of inherited eye diseases and their phenotype-genotype associations.

Keyphrases

optical coherence tomography
diabetic retinopathy
optic nerve
copy number
intellectual disability
autism spectrum disorder