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Eye Syndrome (eye + syndrome)

Distribution by Scientific Domains
Medical Sciences100%

Kinds of Eye Syndrome

  • dry eye syndrome
    		•

    Selected Abstracts

    Anaesthetic management of Cat Eye Syndrome

    PEDIATRIC ANESTHESIA, Issue 6 2001
    Prabhakar Devavaram
    No abstract is available for this article. [source]

    Relationship between eye symptoms and blepharospasm: A multicenter case,control study

    MOVEMENT DISORDERS, Issue 12 2005
    Davide Martino MD
    Abstract Although patients with primary blepharospasm (BSP) commonly report experiencing ocular symptoms before the onset of orbicular spasms, the precise frequency and pathogenic role of this subjective ocular discomfort are poorly understood. We conducted a multicenter case,control study to investigate symptoms related to disorders of the anterior segment of the eye, administering a questionnaire to 165 patients with BSP and 180 age- and gender-matched control patients with hemifacial spasm. On a validation sample, our questionnaire yielded high accuracy in detecting eye diseases (predominantly, dry eye syndrome) using detailed ophthalmological examination as the criterion. Logistic regression analysis indicated a significant association between ocular symptoms at disease onset and BSP. Ocular symptoms starting in the year preceding disease onset (short-latency symptoms) showed a stronger association with BSP than ocular symptoms occurring earlier in time (long-latency symptoms). The association was stronger when short-latency symptoms developed from 40 to 59 years of age, whereas this was not observed for long-latency symptoms. Our findings support the view that eye symptoms associated with BSP result from eye diseases and may be involved in the pathogenesis of BSP. The differential risk of developing BSP, based on age at onset of ocular symptoms, suggests that age and eye diseases may interact in giving rise to BSP. © 2005 Movement Disorder Society [source]

    3221: Pathophysiology of dry eye syndrome

    ACTA OPHTHALMOLOGICA, Issue 2010
    J HORWATH-WINTER
    Dry eye or dysfunctional tear syndrome is a highly prevalent disease worldwide. It is related to a pathological condition of anyone of the parts of the "ocular surface system" that involves the cornea, conjunctiva, lacrimal gland, accessory lacrimal glands, nasolacrimal duct and the lids with the meibomian glands. These are linked as a functional system by innervation, the endocrine and immune system. Endogenous or exogenous caused alterations in one or several components of the ocular surface system or its secretions result in changes of the tear film or ocular surface provoking inflammation. With time, inflammatory reactions may lead to corneal neuropathy compromising the reflex response of the lacrimal glands. Additionally a self-perpetuating vicious circle with loss of function and damage can be initiated also by an immune-modulated inflammation. [source]

    3223: Dry eye syndrome and omega-3 fatty acids

    ACTA OPHTHALMOLOGICA, Issue 2010
    T KAERCHER
    Purpose Dry eye disease is characterized by an inflammatory component of the ocular surface. Pathways to modulate inflammation include corticoids and cyclosporine. Omega-3 fatty acids like eicosapentaenoic acid and docosahexaenoic acid represent an alternate pharmacologic way to influence the inflammatory cascade. Methods Clinical studies. Results An epidemiologic study in 32.470 healthy women showed that those with a higher intake of omega-3 fatty acids had a 68% decreased prevalence of dry eye syndrome. Hyposecretory dry eye was tested after intake of omega-3 fatty acids for 45 days. Symptoms, signs and inflammatory markers like HLA-DR improved. Hyperevaporative dry eye improved after a long-term supplementation with omega-3 fatty acids with respect to symptoms, break-up time and meibom score. Patients with refractive surgery (PRK) improved after omega-3 fatty acids intake; this was derived from the OSDI-score, Schirmer I test and tear clearance. In 102 contact-lens wearers the symptoms and signs of dry eye improved after 12 weeks therapy with omega-3 fatty acids. Conclusion Nutricionals with omega-3 fatty acids show evidence-based effects on the inflammatory component of ocular surface disease and tear film disorder. Their beneficial effect was tested for hypovolemic and hyperevaporative dry eye. Patients after refractive surgery and contact lens wearers improved after supplementation, too. In contrast to the available anti-inflammatory therapy the supplementation is apt for a long-term application. [source]

    2261: Development and evaluation of PLGA nanoparticles with cyclosporine and the inclusion of HP,CD for ocular use

    ACTA OPHTHALMOLOGICA, Issue 2010
    K HERMANS
    Ocular delivery of peptides requires new concepts in order to optimize the bioavailability and its therapeutic effect. The first peptide selected in present research project is Cyclosporine A (CyA) used in the treatment of the dry eye syndrome and against corneal graft rejection. The aim of the project is the development of nanoparticles with physicochemical properties for a suitable and prolonged release of CyA, using a factorial design. These drug delivery systems will be produced employing PLGA using the emulsification solvent evaporation method. Positively charged polymers as chitosan or Eudragit® will be incorporated to obtain nanoparticles with a positive particle charge. Electrostatic interactions with the negatively charged mucins lead to a prolonged residence time at the precorneal area. Nanoparticles will be evaluated on zeta potential, particle size and their in vitro drug release properties. CyA and CyA complexed with HP,CD will be compared. The most suitable preparations will be selected in a next phase of the project for an in vivo study using an animal model. [source]

    Recent developments of dry eye in children

    ACTA OPHTHALMOLOGICA, Issue 2009
    D BREMOND-GIGNAC
    Purpose Dry eye syndrome in children is a rare disease sometimes difficult to diagnose. The research of the etiology can contribute to adjust the treatment. Methods Two features of dry eye syndrome in children can be distinguished. Dry eye integrated in general disease with evidence of diagnosis and etiology and asymptomatic dry eye which needs a careful check up to recognize the primary etiology. Keratitis sicca usually does not lead to children complaint and simple signs as rubbing or blinking are often observed. Clinical and practical cases are described. Results Review of literature confirms common conditions with adult dry eye but also the specificity of the pediatric dry eye. Dry eye in children is also commonly an inflammatory condition of the ocular surface. New treatment with their indications are listed including tear-like topical therapies and anti-inflammatory or immunosuppressive drugs for ocular surface with specificities in children. Conclusion Dry eye syndrome in children must be recognized and diagnosed. In addition to classical tear-like treatment, specific therapy should be adapted to the etiology. [source]

    Structure of the lid margin in laboratory animals

    ACTA OPHTHALMOLOGICA, Issue 2008
    N KNOP
    Purpose The eye lid margin is of great importance for the spreading and the limitation of the tears. The so called lid wiper which is a specialized zone at the inner lid border directly apposed to the corneal surface for spreading the preocular tear film has, at present, only been described for the human conjunctiva. We have investigated common laboratory animals (rat and rabbit) for the presence of such a zone. Methods Conjunctival whole-mount specimens and total bulbi were investigated by serial section histology in ten rats (DA and Lewis) and in ten rabbits (NZW and Chinchilla). Results The stratified squamous keratinised epidermis of the free lid margin showed a sharp transition with loss of the keratin layer at the level of the meibomian glands. Close to the inner lid border it was replaced by a small zone of an optically denser epithelium covered by para-keratinised cells. This area represented the mucocutaneous junction (MCJ) equivalent to the line of Marx in the human. The MCJ rapidly transformed into a thickened 8-12 cell layered stratified epithelium of that formed a cushion-like epithelial elevation, reclined sharply towards the inner lid border and hence formed a typically relatively sharp lip-like edge. The lid-wiper epithelium showed species-specific differences in morphology (cuboidal with goblet cells in the rabbit versus squamous without goblet cells in the rat) but it extended all along the lid margin in both species. Conclusion At the inner border of the upper and lower lid of rat and rabbit, several zones of different morphology occur similar to the human including a lid-wiper structure. Since lid wiper epitheliopathy was shown as a sensitive early indicator for human dry eye syndrome its investigation may be useful for future research in dry eye models of laboratory animals. [source]

    2435: Control of the Meibomian gland in health and disease

    ACTA OPHTHALMOLOGICA, Issue 2010
    DA SULLIVAN
    Purpose The meibomian gland is extremely important in maintaining the health and integrity of the ocular surface. This gland, through its lipid synthesis and secretion, promotes the stability and prevents the evaporation of the tear film. Conversely, meibomian gland dysfunction (MGD) leads to a decreased stability and increased evaporation of the tear film. Indeed, meibomian gland dysfunction is thought to be the major cause of dry eye syndromes throughout the world. Our goal is to advance understanding of the regulation of meibomian gland function and the mechanisms underlying MGD. Methods Procedures included the immortalization of human meibomian gland epithelial cells with human telomerase reverse transcriptase, the evaluation of cellular responsiveness, and the identification of glandular gene expression changes in MGD. Gene analyses were conducted with Illumina HumanHT-12 v3 Expression BeadChips and Geospiza bioinformatics software. Results To date we have [a] immortalized human meibomian gland epithelial cells that respond to secretagogue, growth factor, neurotransmitter and hormone exposure with alterations in proliferation, differentiation, signaling, gene expression and/or lipogenesis; [b] discovered human meibomian gland genes that may facilitate the development and/or progression of MGD. These genes encode proteins that promote keratinization and amplify inflammation. Conclusion Our findings advance our understanding of the control of the meibomian gland in both health and disease. [Acknowledgments: S.M. Richards, M. Hatton, A.M. Fay and K. Lo; Supported by grants from NIH (R01EY05612) and Alcon] Commercial interest [source]