» Articles » PMID: 25309358

Origins of Strabismus and Loss of Binocular Vision

Overview
Date 2014 Oct 14
PMID 25309358
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

Strabismus is a frequent ocular disorder that develops early in life in humans. As a general rule, it is characterized by a misalignment of the visual axes which most often appears during the critical period of visual development. However other characteristics of strabismus may vary greatly among subjects, for example, being convergent or divergent, horizontal or vertical, with variable angles of deviation. Binocular vision may also vary greatly. Our main goal here is to develop the idea that such "polymorphy" reflects a wide variety in the possible origins of strabismus. We propose that strabismus must be considered as possibly resulting from abnormal genetic and/or acquired factors, anatomical and/or functional abnormalities, in the sensory and/or the motor systems, both peripherally and/or in the brain itself. We shall particularly develop the possible "central" origins of strabismus. Indeed, we are convinced that it is time now to open this "black box" in order to move forward. All of this will be developed on the basis of both presently available data in literature (including most recent data) and our own experience. Both data in biology and medicine will be referred to. Our conclusions will hopefully help ophthalmologists to better understand strabismus and to develop new therapeutic strategies in the future. Presently, physicians eliminate or limit the negative effects of such pathology both on the development of the visual system and visual perception through the use of optical correction and, in some cases, extraocular muscle surgery. To better circumscribe the problem of the origins of strabismus, including at a cerebral level, may improve its management, in particular with respect to binocular vision, through innovating tools by treating the pathology at the source.

Citing Articles

Making stereopsis related to the ability of ocular deviation: a new paradigm for assessment of intermittent exotropia.

Li J, Kong W, Shen T, Yuan Y, Chen C, Peng D Int J Ophthalmol. 2025; 18(2):308-314.

PMID: 39967967 PMC: 11754039. DOI: 10.18240/ijo.2025.02.15.


Chromosome 4 Duplication Associated with Strabismus Leads to Gene Expression Changes in iPSC-Derived Cortical Neurons.

Martinez-Sanchez M, Skarnes W, Jain A, Vemula S, Sun L, Rockowitz S Genes (Basel). 2025; 16(1).

PMID: 39858627 PMC: 11764630. DOI: 10.3390/genes16010080.


Maternal Hypertensive Disorder in Pregnancy and Childhood Strabismus in Offspring.

Zhu H, You X, Jing Y, Chen Y, Jiang Y, Lin Y JAMA Netw Open. 2024; 7(7):e2423946.

PMID: 39037813 PMC: 11265127. DOI: 10.1001/jamanetworkopen.2024.23946.


A protocol to quantify cross-sectional and longitudinal differences in duction patterns.

Willeford K, Copel V, Rong H Front Neurosci. 2024; 18:1324047.

PMID: 38919910 PMC: 11196818. DOI: 10.3389/fnins.2024.1324047.


Abnormal occipital and frontal activity during voluntary convergence in intermittent exotropia: A task-fMRI study.

Xia L, Wang Y, Luo S, Zhang Y, Qiu B, Wang X Heliyon. 2024; 10(5):e26197.

PMID: 38495127 PMC: 10943311. DOI: 10.1016/j.heliyon.2024.e26197.


References
1.
White L, Fitzpatrick D . Vision and cortical map development. Neuron. 2007; 56(2):327-38. DOI: 10.1016/j.neuron.2007.10.011. View

2.
Uhlhaas P, Roux F, Singer W, Haenschel C, Sireteanu R, Rodriguez E . The development of neural synchrony reflects late maturation and restructuring of functional networks in humans. Proc Natl Acad Sci U S A. 2009; 106(24):9866-71. PMC: 2687997. DOI: 10.1073/pnas.0900390106. View

3.
Payne B, Siwek D . The visual map in the corpus callosum of the cat. Cereb Cortex. 1991; 1(2):173-88. DOI: 10.1093/cercor/1.2.173. View

4.
Huang P, Li J, Deng D, Yu M, Hess R . Temporal synchrony deficits in amblyopia. Invest Ophthalmol Vis Sci. 2012; 53(13):8325-32. DOI: 10.1167/iovs.12-10835. View

5.
Engle E . Genetic basis of congenital strabismus. Arch Ophthalmol. 2007; 125(2):189-95. DOI: 10.1001/archopht.125.2.189. View