Search results for "Retinal diseases"

showing 10 items of 46 documents

Optical coherence tomography of chorioretinal and choroidal folds

2007

. Purpose:  To report the optical coherence tomography (OCT) findings in cases of chorioretinal and choroidal folds. Methods:  Eight subjects with folds of the fundus of the eye were examined with fundus photography, fluorescein angiography, B-scan ultrasonography and Stratus OCT. Results:  Two types patterns were found on OCT. Five cases showed undulating retinal as well as retinal pigment epithelial lines of normal thickness; these were defined as chorioretinal folds. The posterior vitreous surface often adhered to the crests of the folds only. Three cases exhibited a wavy appearance of the retinal pigment epithelium and a flat retinal surface; these were classified as choroidal folds. Co…

AdultMalevisual acuitygenetic structuresFundus OculiDiagnosis Differentialchemistry.chemical_compoundRetinal DiseasesOptical coherence tomographyPhotographymedicineHumansFluorescein AngiographyPigment Epithelium of EyeAgedChoroidal foldsRetinal pigment epitheliummedicine.diagnostic_testSettore MED/30 - Malattie Apparato Visivobusiness.industryFundus photographyRetinalChoroid DiseasesAnatomyMiddle AgedFluorescein angiographyeye diseasesOphthalmologymedicine.anatomical_structureOCTchemistryFemalesense organsUltrasonographybusinessNormal thicknessTomography Optical CoherenceActa Ophthalmologica Scandinavica
researchProduct

Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary toVPS13Bmutations

2013

Over one hundred VPS13B mutations are reported in Cohen syndrome (CS). Most cases exhibit a homogeneous phenotype that includes intellectual deficiency (ID), microcephaly, facial dysmorphism, slender extremities, truncal obesity, progressive chorioretinal dystrophy, and neutropenia. We report on a patient carrying two VPS13B splicing mutations with an atypical phenotype that included microcephaly, retinopathy, and congenital neutropenia, but neither obesity nor ID. RNA analysis of the IVS34+2T_+3AinsT mutation did not reveal any abnormal splice fragments but mRNA quantification showed a significant decrease in VPS13B expression. RNA sequencing analysis up- and downstream from the IVS57+2T>C…

AdultPathologymedicine.medical_specialtyMicrocephalyNeutropeniaDNA Mutational AnalysisVesicular Transport ProteinsNeutropeniamedicine.disease_causeRetinal DiseasesIntellectual DisabilityGene OrderGeneticsmedicineCongenital Bone Marrow Failure SyndromesHumansObesityCongenital NeutropeniaGenetics (clinical)GeneticsMutationCohen syndromebusiness.industryFaciesSyndromemedicine.diseasePhenotypePedigreeVPS13BPhenotypeMutationFemalebusinessRetinopathyAmerican Journal of Medical Genetics Part A
researchProduct

Congenital hypertrophy of the retinal pigment epithelium and familial polyposis of the colon.

1987

Inquiries to Manuel Diaz Llopis, M.D., Cl Cirilo Amoros No. 1 PTA 2, Valencia 46004, Spain. Familial polyposis of the colon is a dominant autosomal disorder that is characterized by hundreds and sometimes thousands of adenomatous polyps throughout the entire colon, which begin in adolescence. Virtually all pa­ tients with familial polyposis develop carcino­ ma of the colon by age 50 years. A total colectomy should be carried out early in adult life in affected persons. Because of the autosomal dominant inheritance pattern, an intensive sur­ vey of family members must be conducted. There is no phenotype biochemical abnormality or serologic marker that indicates whether a familial member will…

AdultPathologymedicine.medical_specialtyMicrocephalyRetinal pigment epitheliumEpidermal Cystbusiness.industryDiseaseHypertrophymedicine.diseaseMuscle hypertrophySerologyOphthalmologyCongenital hypertrophymedicine.anatomical_structureAdenomatous Polyposis ColiRetinal DiseasesmedicineHumansAbnormalityFluorescein AngiographybusinessPigment Epithelium of EyeAmerican journal of ophthalmology
researchProduct

Retinal myelinated nerve fibers associated with macular pseudohole

2008

We report the case of a 24-year-old woman who presented unilateral extensive peripapillary myelinated nerve fibers associated with macular pseudohole and bilateral low myopia. Visual acuity, slit lamp biomicroscopy, automated perimetry, fundus color photography, and optical coherence tomography (Stratus® OCT) were performed. We discuss the clinical findings and diagnostic details of unilateral extensive peripapillary myelinated nerve fibers associated with macular pseudohole.

AdultVisual acuitygenetic structuresMyelinated nerve fiberNerve fiberEpiretinal membrane Macular pseudohole Oligodendrocytes Retinal myelinated nerve fibersFundus (eye)Nerve Fibers MyelinatedRetinal DiseasesmedicineHumansMacula LuteaFluorescein AngiographyMacular holebusiness.industrySettore MED/30 - Malattie Apparato VisivoOptic NerveAnatomymedicine.diseaseeye diseasesOphthalmologymedicine.anatomical_structureOptic nerveMaculopathyFemalesense organsEpiretinal membranemedicine.symptombusiness
researchProduct

Mitochondrial Markers in Aging and Primary Open-Angle Glaucoma

2020

This review focuses on recent progress in understanding the role of mitochondrial markers in the context of mitochondrial dysfunction in glaucoma and discussing new therapeutic approaches to modulate mitochondrial function and potentially lead to improved outcomes in glaucoma.

AgingMitochondrial Diseasesgenetic structuresOpen angle glaucomabusiness.industryGlaucomaContext (language use)medicine.diseaseBioinformaticseye diseasesOphthalmologyRetinal DiseasesmedicineHumanssense organsbusinessBiomarkersGlaucoma Open-AngleJournal of Glaucoma
researchProduct

Glutathione-dependent formaldehyde dehydrogenase (ADH3) and low km mitochondrial aldehyde dehydrogenase (ALDH2). New evidence for differential expres…

2011

Epidemiological and experimental studies support the involvement of lipid peroxidation (LPO) in retinal diseases. In addition to other pathogenic mechanisms not fully understood, the possibility remains that peroxidic aldehydes, acting as cytotoxic chemicals, mediate in the progression of chronic ocular disorders.To test proper mechanisms involved in removing peroxidic aldehydes from the retina, in an attempt to understand long-lasting changes induced by LPO, the oxidative and antioxidant enzymatic activities, as well as the retinal distribution and activity of glutathione-dependent formaldehyde dehydrogenase (ADH3) and low km mitochondrial aldehyde dehydrogenase (ALDH2), were studied and c…

Aldehyde dehydrogenaseBiologymedicine.disease_causeBiochemistryRetinaLipid peroxidationMitochondrial Proteinschemistry.chemical_compoundRetinal DiseasesmedicineAnimalsRats WistarFormaldehyde dehydrogenaseALDH2Alcohol dehydrogenaseAldehyde Dehydrogenase MitochondrialAlcohol DehydrogenaseRetinalGeneral MedicineGlutathioneAldehyde DehydrogenaseMolecular biologyGlutathioneImmunohistochemistryRatsOxidative StresschemistryBiochemistrybiology.proteinFemaleLipid PeroxidationOxidative stressFree radical research
researchProduct

Distal Arthrogryposis type 5 in an Italian family due to an autosomal dominant gain-of-function mutation of the PIEZO2 gene

2022

Abstract Background Arthrogryposis multiplex congenita (AMC) is a group of clinically and etiologically heterogeneous conditions, characterized by prenatal onset contractures affecting two or more joints. Its incidence is about 1 in 3000 live births. AMC may be distinguished into amyoplasia, distal and syndromic arthrogryposis. Distal arthrogryposis (DA) predominantly affects hands and feet. It is currently divided into more than ten subtypes (DA1, DA2A/B, DA3–10), based on clinical manifestations, gene mutations and inheritance pattern. Among them, only a few patients with DA5 have been reported. It is associated to a gain-of-function pathogenic variant of the PIEZO2 gene, encoding for an …

ArthrogryposisContractureOphthalmoplegiaArthrogryposis multiplex congenita Case report DA5 Gain-of-function mutation NGS Ophthalmoplegia PIEZO2 gene Gain of Function Mutation Humans Infant Newborn Inheritance Patterns Ion Channels Mutation Pedigree Retinal Diseases Arthrogryposis Contracture OphthalmoplegiaRetinal DiseasesGain of Function MutationMutationInfant NewbornInheritance PatternsHumansGeneral MedicineIon ChannelsPedigreeItalian Journal of Pediatrics
researchProduct

Autophagy and mitochondrial alterations in human retinal pigment epithelial cells induced by ethanol: implications of 4-hydroxy-nonenal

2014

Retinal pigment epithelium has a crucial role in the physiology and pathophysiology of the retina due to its location and metabolism. Oxidative damage has been demonstrated as a pathogenic mechanism in several retinal diseases, and reactive oxygen species are certainly important by-products of ethanol (EtOH) metabolism. Autophagy has been shown to exert a protective effect in different cellular and animal models. Thus, in our model, EtOH treatment increases autophagy flux, in a concentration-dependent manner. Mitochondrial morphology seems to be clearly altered under EtOH exposure, leading to an apparent increase in mitochondrial fission. An increase in 2′,7′-dichlorofluorescein fluorescenc…

Cancer ResearchImmunologyApoptosisRetinal Pigment EpitheliumMitochondrionBiologymedicine.disease_causeCell LineLipid peroxidationCellular and Molecular Neurosciencechemistry.chemical_compoundRetinal DiseasesmedicineAutophagyHumanschemistry.chemical_classificationReactive oxygen speciesAldehydesRetinal pigment epitheliumEthanolAutophagyRetinalEpithelial CellsCell BiologyCell biologyMitochondriaOxidative Stressmedicine.anatomical_structurechemistryBiochemistryMitochondrial fissionOriginal ArticleReactive Oxygen SpeciesOxidative stressCell Death & Disease
researchProduct

Color Doppler ultrasonography of the eye and orbit

1993

Color Doppler imaging is the recent development in ultrasonography that allows simultaneous two-dimensional structural imaging in Doppler evaluation of blood flow. With this technique, it is possible for the first time to indirectly display the fine orbital vessels such as the ophthalmic artery and its branches, the central retinal artery, the posterior ciliary artery, and the lacrimal artery. Also, the display of venous structures such as the superior ophthalmic vein, the vortex vein, and the central retinal vein is possible. In addition to the qualitative display of those vessels, the hemodynamics in those vessels can be quantitatively assessed by looking at the Doppler spectrum and deter…

Central retinal arterymedicine.medical_specialtyCentral retinal veinEyechemistry.chemical_compoundRetinal DiseasesCentral retinal vein occlusionmedicine.arteryOphthalmologyOrbital DiseasesmedicineHumansUltrasonographyEquipment Safetybusiness.industryEye NeoplasmsRetinalGeneral Medicinemedicine.diseaseOphthalmologymedicine.anatomical_structurechemistryOphthalmic arterycardiovascular systemLacrimal arteryCentral retinal artery occlusionbusinessOrbitSuperior ophthalmic veinBlood Flow VelocityCurrent Opinion in ophthalmology
researchProduct

Validating retinal fundus image analysis algorithms: issues and a proposal.

2013

This paper concerns the validation of automatic retinal image analysis (ARIA) algorithms. For reasons of space and consistency, we concentrate on the validation of algorithms processing color fundus camera images, currently the largest section of the ARIA literature. We sketch the context (imaging instruments and target tasks) of ARIA validation, summarizing the main image analysis and validation techniques. We then present a list of recommendations focusing on the creation of large repositories of test data created by international consortia, easily accessible via moderated Web sites, including multicenter annotations by multiple experts, specific to clinical tasks, and capable of running …

Computer programFundus OculiCost effectivenessbusiness.industryComputer scienceReproducibility of ResultsContext (language use)Image processingArticlesG400 Computer ScienceReference StandardsSketchOphthalmoscopyConsistency (database systems)SoftwareRetinal DiseasesImage Processing Computer-AssistedHumansbusinessAlgorithmAlgorithmsSoftwareTest data
researchProduct