LAUSR

Oliver McFarlane syndrome and choroidal neovascularisation: a case report

Sign Up to like & get
recommendations!
0 Published in 2020 at "Ophthalmic Genetics"

DOI: 10.1080/13816810.2020.1783689

Abstract: ABSTRACT Background Oliver McFarlane syndrome (OMS) is a rare autosomal recessive disorder characterised by pigmentary chorioretinal atrophy with no previous reports of choroidal neovascularisation (CNV). Material and Methods We describe the history, findings of clinical… read more here.

Keywords: choroidal neovascularisation; case; oliver mcfarlane; mcfarlane syndrome ... See more keywords