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174 Possible Causes for Foveal Atrophy

  • Cone Dystrophy with Supernormal Rod Response

    Macular defects ranging from mild pigmentary changes to distinct foveal atrophy were present in nine patients.[ncbi.nlm.nih.gov] M 17, 36 0.12 5.25 Yes Yes No Slight foveal atrophy Yes 0.12 5.00 14592_IM D339_V341del D339_V341del M 50 0.1 1.50–1.50 135 No Yes No Distinct foveal RPE atrophy ND 0.1 2.50[iovs.arvojournals.org] The fundus appears normal in some patients but foveal or parafoveal atrophy, a macular bull’s eye, hyperfluorescence anomalies, and a generalized fine pigmentary retinopathy[disorders.eyes.arizona.edu]

  • Retinal Telangiectasia

    Fluorescein angiography found no active leakage, and optical coherence tomography found significant foveal atrophy.[ncbi.nlm.nih.gov] Severity 3: Moderate to marked foveal hyperautofluorescence with angiographic abnormalities and foveal atrophy documented on optical coherence tomography.[retinalphysician.com] Nonproliferative perifoveal telangiectasia refers to exudative telangiectasia and foveal atrophy.[scielo.br]

  • Stargardt Disease

    In 14 out of 50 patients, foveal atrophy occurred before flecks developed.[ncbi.nlm.nih.gov] There was a higher prevalence of the variant p.Arg2030Gln in the cohort with foveal sparing compared to the group with foveal atrophy (6.45% vs 1.07%).[ncbi.nlm.nih.gov] RPE atrophy ( asterisks ) was graded as ( B ) none, ( C ) extrafoveal (but not fovea encircling), ( D ) foveal sparing ( 180 encircling the fovea), or ( F ) central RPE atrophy[doi.org]

  • Macular Dystrophy with Central Cone Involvement

    These patients develop foveal atrophy that may be misdiagnosed as Stargardt disease, but the ERG shows severely abnormal photopic responses, whereas the scotopic response[aao.org] The grandfather (II:1) had partial foveal atrophy, with a hyporeflective zone in both eyes.[molvis.org] […] juvenile-onset foveal atrophy surrounded by discrete, yellowish, round or pisciform flecks at the level of the RPE (Fig 12-7A).[quizlet.com]

  • Central Areolar Choroidal Dystrophy

    atrophy surrounded by disciform flecks at the level of the retinal pigment epithelium.[kellogg.umich.edu] This indicates that choriocapillaris atrophy is an early finding in this disease.[ncbi.nlm.nih.gov] […] corresponding to the location of the retinal and retinal pigment epithelium atrophy.[ncbi.nlm.nih.gov]

  • Vitreoretinochoroidopathy

    RESULTS: Long-term follow up of the first ever reported ADVIRC proband revealed progressive foveal atrophy in both eyes 3 decades after his initial presentation.[ncbi.nlm.nih.gov] Fundus autofluorescence photography reveals hypoautofluorescence in the area of foveal retinal pigment epithelial atrophy and mild hyperautofluorescence in the superior, nasal[docksci.com] At age 79, fundus autofluorescence photography demonstrates hypoautofluorescence in the areas of perifoveal retinal pigment epithelial atrophy with hyperautofluorescence in[docksci.com]

  • Achromatopsia

    The younger patients had absent to mild foveal atrophy on OCT, and four of the six demonstrated foveal and parafoveal hyperfluorescence on FAF.[ncbi.nlm.nih.gov] […] in 8.9% of all cases and foveal hypoplasia in 29 patients (85%).[ncbi.nlm.nih.gov] Foveal and outer nuclear layer (ONL) thickness was measured and presence of hypoplasia determined.[ncbi.nlm.nih.gov]

  • Sjogren-Larsson Syndrome

    […] spaces to cystoid foveal atrophy.[ncbi.nlm.nih.gov] CONCLUSIONS: Patients with SLS show a childhood-onset crystalline macular dystrophy with cystoid foveal atrophy on OCT in most cases.[ncbi.nlm.nih.gov] More interestingly, a cystoid foveal degeneration on OCT was present in the majority of patients with SLS (18/27 eyes, or 67% of all eyes studied), varying from multiple microcystoid[ncbi.nlm.nih.gov]

  • Foveal Hypoplasia - Presenile Cataract Syndrome

    Congenital anomaly of eye Congenital nystagmus Foveal hypoplasia Nystagmus Optic atrophy Presenile cataracts Visual impairment Back to: « Foveal hypoplasia Genetics of Foveal[familydiagnosis.com] […] pigmentation and sheathing, retinal thinning, as well as slowly progressive chorioretinal atrophy.[entokey.com] Symptoms of Foveal hypoplasia and presenile cataract syndrome Clinical features : Imported from Human Phenotype Ontology (HPO) Abnormality of the integument Generalized hyperpigmentation[familydiagnosis.com]

  • X-Linked Cone Rod Dystrophy

    These patients develop foveal atrophy that may be misdiagnosed as Stargardt disease, but the ERG shows severely abnormal photopic responses, whereas the scotopic response[aao.org] […] increased foveal in areas of atrophy AF; reduced AF in areas of atrophy severely reduced or undetectable reduced cone and rod responses; * “negative ERG” Peripherin (AD)[entokey.com] […] flash and flicker with minimal or no 30Hz flicker implicit time shift; in CORD, additional reduction in rod responses GUCY2D (AD) 1st, 2nd decade CORD macular and peripheral atrophy[entokey.com]

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