X-linked FRMD7 gene mutation in idiopathic congenital nystagmus and its role in eye movement: A case report and literature review

X-linked FRMD7 gene mutation in idiopathic congenital nystagmus and its role in eye movement: A case report and literature review

BackgroundIdiopathic congenital nystagmus (ICN) is an inherited disorder characterized by uncontrollable binocular conjugating oscillation. X-linked idiopathic congenital nystagmus is one of the most prevalent types of ICN. Elucidation of the genetic mechanisms involved in ICN will enhance our under...

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Bibliographic Details
Main Authors: Fanfei Liu, Minjin Wang, Meng Liao, Longqian Liu, Xiaoshuang Jiang
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-03-01
Series:Frontiers in Ophthalmology
Subjects:
idiopathic congenital nystagmus
FRMD7
X-linked
gene mutation
eye movement
Online Access:https://www.frontiersin.org/articles/10.3389/fopht.2022.1080869/full

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