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PyOKR: A Semi-Automated Method for Quantifying Optokinetic Reflex Tracking Ability
Published on: April 12, 2024
[Molecular genetics advances of congenital idiopathic nystagmus]
Xiao-juan Wang1, Kan-xing Zhao
1Clinical College of Ophthalmology of Tianjin Medical University, Tianjin Eye Hospital and Institute, Tianjin Key Laboratory of Ophthalmology and Visual Science, Tianjin 300020, China.
Abstract:
Congenital idiopathic nystagmus (CIN) is genetically heterogeneous. Autosomal dominant, autosomal recessive and X-linked patterns of inheritance have described. At least three distinct loci are related to autosomal dominant and X-linked patterns. One causative gene for X-linked form has been identified (FRMD7, Xq26.2) through linkage analysis. The molecular genetics advances of the congenital idiopathic nystagmus (CIN) are reviewed.
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