Varied clinical presentations of RP1L1 variants in Chinese patients: a study of occult macular dystrophy and vitelliform macular dystrophy

Abstract Background Occult Macular Dystrophy (OMD), primarily caused by retinitis pigmentosa 1-like 1 (RP1L1) variants, is a complex retinal disease characterised by progressive vision loss and a normal fundus appearance. This study aims to investigate the diverse phenotypic expressions and genotypi...

Volledige beschrijving

Bibliografische gegevens

Hoofdauteurs:	Xiao Liu, Yanling Long, Yu Wang, Bo Liu, Jiayun Ren, Gang wang, Min Wang, Xiaohong Meng, Yong Liu
Formaat:	Artigo
Taal:	Inglês
Gepubliceerd in:	BMC 2024-08-01
Reeks:	BMC Ophthalmology
Onderwerpen:	Occult macular dystrophy RP1L1 gene Phenotypic variability Vitelliform macular dystrophy Chinese patients Genetic analysis
Online toegang:	https://doi.org/10.1186/s12886-024-03591-7
Tags:	Voeg label toe Geen labels, Wees de eerste die dit record labelt!