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

CONCLUSION: 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. PMID: 31266775 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/31266775?dopt=Abstract

Source: The British Journal of Ophthalmology - July 1, 2019 Category: Opthalmology Authors: Hagag AM, Mitsios A, Gill JS, Nunez Do Rio JM, Theofylaktopoulos V, Houston S, Webster AR, Dubis AM, Moosajee M Tags: Br J Ophthalmol Source Type: research