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12 Possible Causes for Subtle Foveal Changes

  • Retinal Telangiectasia

    Similar but more subtle changes were evident in the left eye. What is your diagnosis?[maculaspecialists.com.au] Examination of the right macula revealed an altered foveal reflex with slight loss of retinal transparency temporal to the fovea (Figure 1).[maculaspecialists.com.au] Differential diagnosis The differential diagnosis of an altered foveal and parafoveal reflex in a middle aged male is extensive, but includes: Central serous chorioretinopathy[maculaspecialists.com.au]

  • Toxic Retinopathy

    In our case, the retinal changes only seen on FAF were very subtle in the foveal and macular area and were mainly in the area outside the arcades, mainly inferiorly, and very[karger.com] The earliest clinical changes in HCQ retinopathy are subtle changes at the macula, with pigmentary stippling and loss of the foveal reflex (the typical light reflection seen[academic.oup.com]

  • Foveal Retinoschisis

    Retinoschisis is hard to diagnose in patient with subtle macula change and hyperopic amblyopia.[ncbi.nlm.nih.gov] We report a case of bilateral foveal retinoschisis before and after treatment with topical dorzolamide, which was misdiagnosed as bilateral hyperopic amblyopia.[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 30

    Indeed, the multifocal ERG can be grossly abnormal even when ophthalmoscopic changes are absent or subtle (12), as in our Case 1.[journals.lww.com] Although full-field ERG is widely available and is abnormal once ophthalmoscopic changes have become apparent (10), multifocal ERG may be more sensitive for detecting foveal[journals.lww.com]

  • Amblyopia

    Retinoschisis is hard to diagnose in patient with subtle macula change and hyperopic amblyopia.[ncbi.nlm.nih.gov] We report a case of bilateral foveal retinoschisis before and after treatment with topical dorzolamide, which was misdiagnosed as bilateral hyperopic amblyopia.[ncbi.nlm.nih.gov]

  • Cystoid Macular Dystrophy

    Stage O Premacular hole- Perifoveal vitreous detachment - Loss of foveal depression - Subtle macular topograph changes - Normal visual acuity 8.[docslide.com.br] Stage 1a: Impending macular hole- flattening of the foveal depression with an underlying yellow spot. - Pseudocyst a perifoveal vitreoretinal detachment Pathology: inner retinal[docslide.com.br]

  • Goldmann-Favre Syndrome

    […] pigmentary changes and areas of hyperpigmentation within the vascular arcades associated with increased AF on FAI.[iovs.arvojournals.org] Foveal schisis is demonstrated on OCT; ( c ) patient 2, areas of hyperpigmentation within the vascular arcades associated with increased AF on FAI; ( d ) patient 5, nummular[iovs.arvojournals.org] […] clinical phenotype. ( a ) Patient 4, subtle pigmentary changes along the vascular arcades, with an absence of AF outside the arcades; ( b ) patient 14, macular disturbance with subtle[iovs.arvojournals.org]

  • Retinitis Pigmentosa 26

    changes by two independent observers (W.I. and Z.E.).[djo.eg.net] Foveal atrophy was defined as CMT at 1-mm Early Treatment Diabetic Retinopathy Study circle less than or equal to180 µm.[djo.eg.net] […] evaluation of vitreomacular interface, outer retinal layers, inner segment-outer segment (IS-OS) junction, and retinal pigment epithelium (RPE) was carried out to reveal subtle[djo.eg.net]

  • Retinitis Pigmentosa 32

    changes by two independent observers (W.I. and Z.E.).[djo.eg.net] Foveal atrophy was defined as CMT at 1-mm Early Treatment Diabetic Retinopathy Study circle less than or equal to180 µm.[djo.eg.net] […] evaluation of vitreomacular interface, outer retinal layers, inner segment-outer segment (IS-OS) junction, and retinal pigment epithelium (RPE) was carried out to reveal subtle[djo.eg.net]

  • Aniridia

    METHODS: Retrospective case series of patients diagnosed with a subtle aniridia phenotype characterized by minimal iris abnormalities, foveal hypoplasia, and an identified[ncbi.nlm.nih.gov] Here, we present six families with a history of low vision/blindness with a previously undiagnosed mild aniridia phenotype with minimal iris changes.[ncbi.nlm.nih.gov]

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