EPOS

European Paediatric Ophthalmological Society

Annual Meeting 2007 - Abstracts

The final programme of the meeting: Download the final programme (ca. 161 kb)

Abstracts of all talks

Andersson Susann: Unilateral Pigmentary Retinopathy -a follow-up case report

Andersson Grönlund Marita: Electrophysiological findings in children and young adults with genetically verified mitochondrial diseases

Audren Francois: Screening of retinal toxicity of hydroxychloroquine and chloroquine in children

Austeng Dordi: Visual perseption impairment in infants born very preterm.

Aznauryan Igor: Parameters of visual evoked potentials as an evaluation criterion of the treatment efficiency of children’s opticochiasmatic arachnoiditis

Balasanyan Viktorya: Binocular optometric complex

BRECELJ JELKA: SIMULTANEOUS ERG AND VEP RECORDING IN INFANTS AND YOUNG CHILDREN

Bredrup Cecilie: The eye in Pierson syndrome

BREMOND-GIGNAC Dominique: Imaging of anterior segment in the management and the comprehension of ocular dysgenesia

Català Mora Jaume: X-LINKED RETINOSCHISIS: UTILITY OF ELECTRORETINOGRAM AND OCT IN THE DIAGNOSIS OF PEDIATRIC MACULOPATHIES

Coeckelbergh Tanja: What determines the choice of a PRL?

de veuster ilse: Left hemianopia in a 10 th month old child. Pieces of puzzle.

Di Pietro Massimo: Infrequent cases in pediatric ophthalmology

Dollfus Hélène: Ciliopathies in ophthalmology

DUREAU Pascal: Evolutivity of persistent fetal vasculature

edelson catherine: Bimanual microincision cataract surgery in pediatric patients under 6 months of age

Fomina Natalya: Retinopathy of Prematurity in infants with birth weight of 501g to 750 g.

Friedburg Christoph: Spectrum of the ocular phenotype associated with the P193L-Mutation of RS1

Fulton Anne: Development of Retinal Responses:From Molecules to Diagnosis

Funnell Charlotte: Neodymium Yttrium Aluminium Garnet (Nd: YAG) Laser versus Surgical Capsulotomy following Paediatric Cataract Surgery – A Retrospective Study of 106 Eyes

Hamilton Ruth: The step VEP acuity test in suspected functional visual acuity loss

Harris Christopher: Measuring Horizontal Saccade Speed from Non-Intructable Children And Infants

Holder Graham: ERGs in inherited retinal disease

Holmstrom Gerd: SWEDROP- A Swedish register for ROP

Jaeger Melanie: Correlation of abnormal fundus autofluorescence with visual function

Jarc-Vidmar Martina: Clinical and genetic heterogenity in two Slovene families with Best vitelliform dystrophy

Kalhoro Ambreen: Congenital macular atrophy in association with high myopia

Koch Martina: Visual loss 6 years after congenital glaucoma operation

KOOIJMAN DE GROOT MARJOLEIN: The first outcomes of treatment for ROP in a new paediatric vitroretinal centre

Kozeis Nikolaos: Visual resolution, color perception & contrast sensitivity in cerebral palsied children

Kozeis Nikolaos: Visual resolution vs. ERG & VEP in cerebral palsied children

Kozeis Nikolaos: Brain damage, VEPs & BAEP in cerebral palsied children

Kozeis Nikolaos: VEPs –brain MRI & epilepsy in cerebral palsy

Larsson Eva: The macular and retinal nerve fibre layer thickness, assessed with OCT and HRT, in full-term children aged 5-16 years.

Larsson Eva: Population-based long-term follow-up of prematurely-born children previously screened for ROP.

Leyssens Barbara: Treatment of exudative changes in Coat’s type retinitis pigmentosa

Lorenz Birgit: Update on the molecular causes of congenital nystagmus

Malik Aeesha: Familial B cell Immunodeficiency (hypogammaglobulinaemia), infantile cataracts and short stature in 3 siblings- a new autosomal recessive disorder?

Malik Aeesha: Varied Clinical Presentation of Viral Stromal Keratitis in Children

MATHEW Rashmi: Congenital Coloboma: new presentations to a district general hospital

Miller Marilyn T: Childhood Blindness: A Worldwide Perspective

Miller Marilyn T: Aberrant Tearing Associated with other Cranial Nerve Dysfunction: An Insight into an Abnormal Neurodevelopment?

Molenaar Esther: “Case Report: An infant with Neurofibromatosis type 2 presenting with meningioma and combined pigment epithelial and retinal hamartoma”

Moore Anthony: Cone and cone-rod dystrophies, genotype, phenotype and disease mechanisms.

Morales Marta: Visual outcomes after primary intraocular lens implantation in developmental pediatric cataracts.

Moser Elisabeth: Bilateral congenital cataract and severe developmental delay - a case of Warburg Micro Syndrome?

Özmen Ahmet: Results of postoperative corneal astigmatism in pediatric cataract surgery

Petrinovic Doresic Jelena: Retinopathy of prematurity (ROP) service in Croatia – standing on the top of a slippery iceberg

Porro Giorgio: Visual functions in children after epilepsy surgery

Pott Jan Willem: Bradyopsia; clinical features and follow-up

Prat Joan: Clinical and CT manifestations in orbital cellulitis

Preising Markus: Molecular Genetic Screening of Patients with Albinism for Mutations in P-Gene and TYR, and OA1

roulez francoise: Corneal dystrophy in the Hallermann-Streiff syndrome

Schalij-Delfos Nicoline: Poor vision from birth: the value of electrofysiological investigation.

Schalij-Delfos Nicoline: The use of the Optical Coherent Tomography (OCT) in the assessment of macular edema in infants with uveitis.

Schuil José: Oculocutaneous albinism and proportional growth failure in a girl with a deletion of region 15q.26

Spasovska Katerina: Interleukin-6 review in the blood of Preterm Infants with Sepsis who develop Retinopathy of Prematurity (ROP)

Sterner Bertil: Reliability in examination of the amplitude of accommodation

Sturm Veit: Ophthalmological manifestations in LCHAD deficiency: presentation of a longitudinal reanalysis of a long-term survivor

Šuštar Maja: Full-field and ON-OFF ERG abnormalities in children with CSNB

Taylor David: Listen, Look, Think- make diagnoses!

Tekavcic Pompe Manca: CHROMATIC VEP TO RED-GREEN STIMULATION IN CHILDREN WITH CONGENITAL COLOUR VISION DEFICIENCY

Thompson Dorothy: Invited presentation. VEPs in Infants and Children - how can they help?

Thyagarajan Sri: Cone dystrophies and partial cone dysfunction presenting to Great Ormond Street Hospital for Children

van Genderen Maria: A novel condition, consisting of mild anterior segment anomalies, chiasmal misrouting, and foveal hypoplasia, maps to a locus on chromosome 16q

Verb Stephen: Orbital Cellulitis in Children

Wolley Dod Charlotte: Lacrimal Gland Agenesis: a two case report