| L/P/C |
Author |
Abstract-Title |
Friday, 12:00 - 2:00pm
Registration
Friday, 2:00pm
Opening
Friday, 2:15 pm |
| L |
Michael Baraitser |
The eye in
the Dysmorphology Databases. |
| L |
Kerstin Strömland |
Using ocular
dysmorphology and associated anomalies in timing birth defects
in syndromes. |
| SP |
Eduardo Silva |
Defining the minimal
critical region for the Peters plus syndrome. |
| C |
Badia Fahad |
Cranio-ectodermal
dysplasia - Sensenbrenner syndrome: A case presentation. |
| C |
Christopher Williams |
A New Case of
ocular abnormalities and "Apple-Peel" intestinal atresia with
multiple variable aneuploidy |
| C |
Shauna Quinn |
Autosomal dominant
brachydactyly, coloboma and anterior segment dysgenesis. |
| C |
Jin Hong |
Bilateral Peters
anomaly, failure to thrive and primary hypoaldosteronism. |
| C |
Lilianne Duarte |
Hypomelanosis
of Ito. Case report. |
| C |
Bettina Wabbels |
An unusual case
of complex ocular and eyelid malformations. |
| C |
Pedro Faria |
Bilateral congenital
anophthalmia with cyst associated with severe neurodegeneration.
A new syndrome or association? |
| Friday, 4:45pm |
| L |
Veronica van Heyningen |
Transcription
factors and eye development. |
| L |
Elfride De Baere |
FOXL2 AND BPES:
mutational hotspots, intrafamilial variability and revision
of genotype-phenotype correlation. |
| P |
Hélène Dollfus |
FOXL2 and TWIST
mutations in families with developmental anomalies of the
eyelids. |
| P |
Stella Hornby |
Aetiology of
ocular coloboma in South India. |
| C |
Peter Hodgkins |
Papillo-renal
syndrome: A new PAX2 mutation. |
| C |
João Rodrigues |
Coloboma: clinical
cases. |
| P |
Mary J. van Schooneveld |
Morning glory
syndrome. |
Saturday, 8:00am Registration
Saturday, 8:30am |
| L |
Dagmar Wieczorek |
Call for patients
- The Oculo-Auriculo-Vertebral Spectrum (OAVS) - a clinical
and molecular project. |
| C |
Ana Xavier |
A case of Moebius-Poland
sequence: where did it start? |
| C |
Teresa Torrent |
Moebius-like
syndrome or another diagnostic challenge. |
| C |
Michael Michaelides |
A Novel case
of Hypertelorism, Hypospadias, Strabismus and bilateral Congenital
Lacrimal Fistulae |
| C |
Tae Yoon La |
A Case of Patau Syndrome with
Congenital Ocular Anomaly |
| C |
Rosa Sust |
Wolf-Hirschhorn-Like
Syndrome associated with a complex rearrangement of chromosome
4. |
| C |
Ingele Casteels |
Familial inherited
microtia, ocular colobomas and imperforation of the nasolacrimal
ducts with abnormal chromosome condensation on 4p16.1. |
| C |
Ligia Cardoso |
Just another
case of cerebral palsy or beyond? |
| Saturday, 10:30am |
| P |
Irene Maumanee |
Finding Genes in
Leber Congenital Amaurosis |
| P |
Markus Preising |
Screening of NUB1 in Patients
with Leber congenital amaurosis. |
| P |
Astrid Plomp |
Does autosomal
dominant pseudoxanthoma elasticum exist? |
| P |
Marie-Claire Gaillard |
Heterogeneity
of retinal degeneration in cobalamin C disease methylmalonic
aciduria with homocystinuria. |
| P |
Hansjörg Soeldner |
Retinal dystrophy
in long chain 3-hydroxy-acyl-coA dehydrogenase deficiency |
| C |
Michel Michaelides |
Oligocone Trichromacy |
| C |
Augusto Magalhães |
Ocular aspects
of Aicardi's syndrome. |
| Saturday, 12:00am |
| BOARD MEETING |
| Saturday, 2:30pm |
| P |
Caroline Gardiner |
Cataract extraction
+/- intraocular lens implantation in a series of infants and
children with Down's syndrome. |
| P |
Joaquim N Murta |
Traumatic cataract
in children. Functional results. |
| P |
Isabel Prieto |
Pediatric cataracts
: our surgical experience. |
| SP |
Joaquim N Murta |
Cataract surgery
in children with uveitis. |
| P |
Filomena Ribeiro |
Uveitis in children. |
| SP |
Branka Stirn Kranjc |
Orbital myositis. |
| C |
Michael O'Keefe |
Choroidal haemangioma
associated with Sturge-Weber Syndrome treated with low dose
ocular irradiation. |
| P |
M. Schittkowski |
Treatment of
congenital anophthalmos with self-inflating hydrogel expanders. |
| P |
Christoph Hintschich |
Enucleation
in childhood - a threat for bony orbital development in humans? |
| C |
Catherine G Brozou |
Macrophthalmus associated
with Neurofibromatosis type 1 |
| Saturday, 5:00pm |
| P |
Nel Tijmes |
A survey of the
visual performance of mentally disabled people in institutions. |
| P |
Sajid Khan |
Visual outcomes
and amblyogenic risk factors in syndromic craniosynostosis
- a review of 141 cases. |
| P |
Pierre Bitoun |
Autism in congenitally
blind children? Genetic or environmental. |
| P |
Marita Andersson Grönlund |
Visual function
and ocular morphology in healthy term children from 4 to 16
years. |
| C |
Eva Aring |
Orthoptic findings In healty
term children from 4 To 16 years |
| P |
Susann Andersson |
Visual acuity
and visual perception in children with operated hydrocephalus. |
| P |
Elisabeth Moser |
Cohen Syndrome
- a possible differential diagnosis in retarded children with
high myopia. |
| Sunday, 9:00am |
| P |
Susana Teixeira |
Retinopathy
of Prematurity: a retrospective case-control study in a neonatal
intensive care unit. |
| P |
Natalya Fomina |
The main risk
factors for IV-V stages of Retinopathy of Prematurity. |
| P |
Gerd Holmström |
Incidence of
ROP in two consecutive Swedish population-based studies. |
| SP |
Eva Larsson |
Peripheral and
central visual fields in prematurely born children and in
full-term controls |
| C |
Maria João Santos |
Coats' disease - a clinical
case |
| SP |
Catherine Marsh |
Unilateral PHPV:
A series of cases. |
| C |
Nicoline Schalij-Delfos |
Uncommon presentation
of retinoblastoma. |
| Sunday, 11:00am |
| C |
Sharola Dharmaraj |
Ocular findings
in proximal trisomy 1q mosaicism |
| C |
Susana Teixeira |
Facial and orbital haemangioma
associated to an intracranial complex vascular malformation
- Case Report |
| C |
Fernando Trancoso Vaz |
Unifocal Langerhans' Cell
Histiocytosis |
| C |
Concepcion Ferrer Novella |
Hurler Syndrome:
Early diagnosis starting from ophthalmological manifestations |
| C |
Sonia Campos |
Bilateral retinal
dysplasia, developmental delay and autistic behaviour in two
brothers. Another challenging case report. |
| P |
Ayd Shafiq |
Linkage analysis
in a Liverpool family with dominantly inherited microcornea
and cataract. |
| C |
Jorge Breda |
Ocular manifestations
of congenital sleep disease. |
| P |
Susana Teixeira |
Paediatric AIDS |
| C |
Inmaculada González Viejo |
Ectropion uveae: Clinical
manifestations |
| Sunday, 12:30pm Closing |
