Clinical and genetic studies for a cohort of patients with congenital stationary night blindness

Abstract Background Congenital stationary night blindness (CSNB) is an inherited retinal disorder. Most of patients have myopia. This study aims to describe the clinical and genetic characteristics of fifty-nine patients with CSNB and investigate myopic progression under genetic cause. Results Sixty...

Full description

Bibliographic Details
Main Authors: Lijuan Huang, Xueqing Bai, Yan Xie, Yunyu Zhou, Jin Wu, Ningdong Li
Format: Article
Language:English
Published: BMC 2024-03-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Online Access:https://doi.org/10.1186/s13023-024-03091-3