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Optic nerve hypoplasia

Optic nerve hypoplasia (ONH) is a congenital anomaly of the optic disc that might result in moderate to severe vision loss in children. With a vast number of cases now being reported, the rarity of ONH is obviously now refuted. The major aspects of ophthalmic evaluation of an infant with possible ON...

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Autores principales: Kaur, Savleen, Jain, Sparshi, Sodhi, Harsimrat B. S., Rastogi, Anju, Kamlesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779419/
https://www.ncbi.nlm.nih.gov/pubmed/24082663
http://dx.doi.org/10.4103/0974-620X.116622
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author Kaur, Savleen
Jain, Sparshi
Sodhi, Harsimrat B. S.
Rastogi, Anju
Kamlesh,
author_facet Kaur, Savleen
Jain, Sparshi
Sodhi, Harsimrat B. S.
Rastogi, Anju
Kamlesh,
author_sort Kaur, Savleen
collection PubMed
description Optic nerve hypoplasia (ONH) is a congenital anomaly of the optic disc that might result in moderate to severe vision loss in children. With a vast number of cases now being reported, the rarity of ONH is obviously now refuted. The major aspects of ophthalmic evaluation of an infant with possible ONH are visual assessment, fundus examination, and visual electrophysiology. Characteristically, the disc is small, there is a peripapillary double-ring sign, vascular tortuosity, and thinning of the nerve fiber layer. A patient with ONH should be assessed for presence of neurologic, radiologic, and endocrine associations. There may be maternal associations like premature births, fetal alcohol syndrome, maternal diabetes. Systemic associations in the child include endocrine abnormalities, developmental delay, cerebral palsy, and seizures. Besides the hypoplastic optic nerve and chiasm, neuroimaging shows abnormalities in ventricles or white- or gray-matter development, septo-optic dysplasia, hydrocephalus, and corpus callosum abnormalities. There is a greater incidence of clinical neurologic abnormalities in patients with bilateral ONH (65%) than patients with unilateral ONH. We present a review on the available literature on the same to urge caution in our clinical practice when dealing with patients with ONH. Fundus photography, ocular coherence tomography, visual field testing, color vision evaluation, neuroimaging, endocrinology consultation with or without genetic testing are helpful in the diagnosis and management of ONH. (Method of search: MEDLINE, PUBMED).
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spelling pubmed-37794192013-09-30 Optic nerve hypoplasia Kaur, Savleen Jain, Sparshi Sodhi, Harsimrat B. S. Rastogi, Anju Kamlesh, Oman J Ophthalmol Review Article Optic nerve hypoplasia (ONH) is a congenital anomaly of the optic disc that might result in moderate to severe vision loss in children. With a vast number of cases now being reported, the rarity of ONH is obviously now refuted. The major aspects of ophthalmic evaluation of an infant with possible ONH are visual assessment, fundus examination, and visual electrophysiology. Characteristically, the disc is small, there is a peripapillary double-ring sign, vascular tortuosity, and thinning of the nerve fiber layer. A patient with ONH should be assessed for presence of neurologic, radiologic, and endocrine associations. There may be maternal associations like premature births, fetal alcohol syndrome, maternal diabetes. Systemic associations in the child include endocrine abnormalities, developmental delay, cerebral palsy, and seizures. Besides the hypoplastic optic nerve and chiasm, neuroimaging shows abnormalities in ventricles or white- or gray-matter development, septo-optic dysplasia, hydrocephalus, and corpus callosum abnormalities. There is a greater incidence of clinical neurologic abnormalities in patients with bilateral ONH (65%) than patients with unilateral ONH. We present a review on the available literature on the same to urge caution in our clinical practice when dealing with patients with ONH. Fundus photography, ocular coherence tomography, visual field testing, color vision evaluation, neuroimaging, endocrinology consultation with or without genetic testing are helpful in the diagnosis and management of ONH. (Method of search: MEDLINE, PUBMED). Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3779419/ /pubmed/24082663 http://dx.doi.org/10.4103/0974-620X.116622 Text en Copyright: © 2013 Kaur S, et al. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review Article
Kaur, Savleen
Jain, Sparshi
Sodhi, Harsimrat B. S.
Rastogi, Anju
Kamlesh,
Optic nerve hypoplasia
title Optic nerve hypoplasia
title_full Optic nerve hypoplasia
title_fullStr Optic nerve hypoplasia
title_full_unstemmed Optic nerve hypoplasia
title_short Optic nerve hypoplasia
title_sort optic nerve hypoplasia
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779419/
https://www.ncbi.nlm.nih.gov/pubmed/24082663
http://dx.doi.org/10.4103/0974-620X.116622
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