Isolated foveal hypoplasia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
http://link.springer.com/content/pdf/10.1007/s10792-008-9215-5.pdf
Reference12 articles.
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2. Meyer CH, Lapolice DJ, Freedman SF (2002) Foveal hypoplasia in oculocutaneous albinism demonstrated by optical coherence tomography. Am J Ophthalmol 133:409–410
3. Gehring WJ (1996) The master control gene for morphogenesis and evolution of the eye. Genes Cells 1:11–15
4. Ton CCT, Hirvonen H, Miwa H, Weil MM, Monaghan P, Jordan T et al. (1991) Positional cloning and characterization of a paired box and homeobox-containing gene from the aniridia region. Cell 67:1059–1074
5. Oliver MD, Dotan SA, Chemke J, Abraham FA (1987) Isolated foveal hypoplasia. Br J Ophthalmol 71:926–930
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1. Multimodal phenotyping of foveal hypoplasia in albinism and albino-like conditions: a pediatric case series with adaptive optics insights;Scientific Reports;2024-07-04
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3. Incidence and clinical significance of fovea plana in the French population with age-related cataract;European Journal of Ophthalmology;2022-12-25
4. Microperimetry assessment in foveal hypoplasia: functional results in a series of pediatric patients;Canadian Journal of Ophthalmology;2022-11
5. Bilateral isolated foveal hypoplasia without nystagmus;Egyptian Retina Journal;2021
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