Foveal hypoplasia is a retinal disorder in which there is a lack of full development of the morphology of the fovea. The optical coherence tomography (OCT) and functional findings are presented in relation to the underlying genetic and developmental conditions. Recent advancements of high-resolution OCT imaging have unveiled characteristics of foveal hypoplasia that were not detected by conventional imaging methods. An absence of a foveal pit does not necessarily imply poor visual acuity, and the maturation of the cone photoreceptors is important for the visual acuity. Regardless of the degree of the development of the inner retinal layers, the visual acuity can be preserved as in diseases such as Stickler syndrome that is a newly identifie...
Usually associated with other ocular anomalies, isolated foveal hypoplasia is a rare developmental d...
ta am 38 is g cular zone, absent or abnormal foveal and/or macular the UCSC Genome Browser (Table S1...
AbstractAlbinism, an inherited disorder of melanin biosynthesis, disrupts normal retinal development...
ObjectivesTo elucidate the visual significance of the foveal pit by measuring foveal architecture an...
AIMS: To discuss foveal development in the context of detailed retinal vasculature imaging in foveal...
Foveal hypoplasia is a retinal disorder in which the foveal pit of the macula lutea is incompletely ...
Purpose: To determine the prevalence and characteristics of foveal hypoplasia (also called fovea pla...
Background. Foveal hypoplasia is characterized by the lack of a defined foveal depression with prese...
We present handheld optical coherence tomography (OCT) diagnosis of Grade 4 foveal hypoplasia (fovea...
Abstract Purpose To describe a patient with isolated foveal hypoplasia. Methods A 55-year-old man wi...
Purpose To investigate the optic nerve and macular morphology in patients with optic nerve hypoplasi...
Background: Down syndrome is a common multigene, multisystem disorder associated with abnormalities ...
PurposeTo investigate the optic nerve and macular morphology in patients with optic nerve hypoplasia...
The purpose of this report is to describe a case of bilateral foveal hypoplasia in the absence of ot...
Background/aims: To present the ophthalmological and electropnysiological characteristics of three d...
Usually associated with other ocular anomalies, isolated foveal hypoplasia is a rare developmental d...
ta am 38 is g cular zone, absent or abnormal foveal and/or macular the UCSC Genome Browser (Table S1...
AbstractAlbinism, an inherited disorder of melanin biosynthesis, disrupts normal retinal development...
ObjectivesTo elucidate the visual significance of the foveal pit by measuring foveal architecture an...
AIMS: To discuss foveal development in the context of detailed retinal vasculature imaging in foveal...
Foveal hypoplasia is a retinal disorder in which the foveal pit of the macula lutea is incompletely ...
Purpose: To determine the prevalence and characteristics of foveal hypoplasia (also called fovea pla...
Background. Foveal hypoplasia is characterized by the lack of a defined foveal depression with prese...
We present handheld optical coherence tomography (OCT) diagnosis of Grade 4 foveal hypoplasia (fovea...
Abstract Purpose To describe a patient with isolated foveal hypoplasia. Methods A 55-year-old man wi...
Purpose To investigate the optic nerve and macular morphology in patients with optic nerve hypoplasi...
Background: Down syndrome is a common multigene, multisystem disorder associated with abnormalities ...
PurposeTo investigate the optic nerve and macular morphology in patients with optic nerve hypoplasia...
The purpose of this report is to describe a case of bilateral foveal hypoplasia in the absence of ot...
Background/aims: To present the ophthalmological and electropnysiological characteristics of three d...
Usually associated with other ocular anomalies, isolated foveal hypoplasia is a rare developmental d...
ta am 38 is g cular zone, absent or abnormal foveal and/or macular the UCSC Genome Browser (Table S1...
AbstractAlbinism, an inherited disorder of melanin biosynthesis, disrupts normal retinal development...