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Case report: Unilateral optic nerve aplasia and developmental hemi-chiasmal dysplasia with VEP misrouting

PURPOSE: To describe the trans-occipital asymmetries of pattern and flash visual evoked potentials (VEPs), in an infant with MRI findings of unilateral optic nerve aplasia and hemi-chiasm dysplasia. METHODS: A child with suspected left cystic microphthalmia, left microcornea, left unilateral optic n...

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Autores principales: Handley, Sian E., Marmoy, Oliver R., Gore, Sri K., Mankad, Kshitij, Thompson, Dorothy A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943516/
https://www.ncbi.nlm.nih.gov/pubmed/32852652
http://dx.doi.org/10.1007/s10633-020-09788-7
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author Handley, Sian E.
Marmoy, Oliver R.
Gore, Sri K.
Mankad, Kshitij
Thompson, Dorothy A.
author_facet Handley, Sian E.
Marmoy, Oliver R.
Gore, Sri K.
Mankad, Kshitij
Thompson, Dorothy A.
author_sort Handley, Sian E.
collection PubMed
description PURPOSE: To describe the trans-occipital asymmetries of pattern and flash visual evoked potentials (VEPs), in an infant with MRI findings of unilateral optic nerve aplasia and hemi-chiasm dysplasia. METHODS: A child with suspected left cystic microphthalmia, left microcornea, left unilateral optic nerve aplasia, and hemi-chiasm underwent a multi-channel VEP assessment with pattern reversal, pattern onset, and flash stimulation at the age of 16 weeks. RESULTS: There was no VEP evidence of any post-retinal visual pathway activation from left eye with optic nerve aplasia. The VEP trans-occipital distribution from the functional right eye was skewed markedly across the midline, in keeping with significant misrouting of optic nerve fibres at the chiasm. This was supported by the anatomical trajectory of the optic chiasm and tracts seen on MRI. CONCLUSION: This infant has chiasmal misrouting in association with unilateral optic nerve aplasia and unilateral microphthalmos. Chiasmal misrouting has not been found in patients with microphthalmos or anophthalmos, but has been reported after early eye loss in animal models. Our findings contribute to our understanding of the discrepancy between the visual pathway physiology of human unilateral microphthalmia and animal models.
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spelling pubmed-79435162021-03-28 Case report: Unilateral optic nerve aplasia and developmental hemi-chiasmal dysplasia with VEP misrouting Handley, Sian E. Marmoy, Oliver R. Gore, Sri K. Mankad, Kshitij Thompson, Dorothy A. Doc Ophthalmol Clinical Case Report PURPOSE: To describe the trans-occipital asymmetries of pattern and flash visual evoked potentials (VEPs), in an infant with MRI findings of unilateral optic nerve aplasia and hemi-chiasm dysplasia. METHODS: A child with suspected left cystic microphthalmia, left microcornea, left unilateral optic nerve aplasia, and hemi-chiasm underwent a multi-channel VEP assessment with pattern reversal, pattern onset, and flash stimulation at the age of 16 weeks. RESULTS: There was no VEP evidence of any post-retinal visual pathway activation from left eye with optic nerve aplasia. The VEP trans-occipital distribution from the functional right eye was skewed markedly across the midline, in keeping with significant misrouting of optic nerve fibres at the chiasm. This was supported by the anatomical trajectory of the optic chiasm and tracts seen on MRI. CONCLUSION: This infant has chiasmal misrouting in association with unilateral optic nerve aplasia and unilateral microphthalmos. Chiasmal misrouting has not been found in patients with microphthalmos or anophthalmos, but has been reported after early eye loss in animal models. Our findings contribute to our understanding of the discrepancy between the visual pathway physiology of human unilateral microphthalmia and animal models. Springer Berlin Heidelberg 2020-08-27 2021 /pmc/articles/PMC7943516/ /pubmed/32852652 http://dx.doi.org/10.1007/s10633-020-09788-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical Case Report
Handley, Sian E.
Marmoy, Oliver R.
Gore, Sri K.
Mankad, Kshitij
Thompson, Dorothy A.
Case report: Unilateral optic nerve aplasia and developmental hemi-chiasmal dysplasia with VEP misrouting
title Case report: Unilateral optic nerve aplasia and developmental hemi-chiasmal dysplasia with VEP misrouting
title_full Case report: Unilateral optic nerve aplasia and developmental hemi-chiasmal dysplasia with VEP misrouting
title_fullStr Case report: Unilateral optic nerve aplasia and developmental hemi-chiasmal dysplasia with VEP misrouting
title_full_unstemmed Case report: Unilateral optic nerve aplasia and developmental hemi-chiasmal dysplasia with VEP misrouting
title_short Case report: Unilateral optic nerve aplasia and developmental hemi-chiasmal dysplasia with VEP misrouting
title_sort case report: unilateral optic nerve aplasia and developmental hemi-chiasmal dysplasia with vep misrouting
topic Clinical Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943516/
https://www.ncbi.nlm.nih.gov/pubmed/32852652
http://dx.doi.org/10.1007/s10633-020-09788-7
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