09.12.2012 Views

Table of Contents - WOC 2012

Table of Contents - WOC 2012

Table of Contents - WOC 2012

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

<strong>WOC</strong><strong>2012</strong> Abstract Book<br />

Pediatric Ophthalmology, Genetics<br />

PO-PED-01<br />

Apropose two cases <strong>of</strong> coloboma <strong>of</strong> the eyelid in the oculo-frontocutaneous<br />

syndrome<br />

Le Do Thuy Lan (1)<br />

1. University <strong>of</strong> Medicine Pham Ngoc Thach<br />

Objectives: Coloboma <strong>of</strong> the eyelid is able to associate with choristoma,<br />

especially in syndromes about complexe anomalies. The authors analyzed two<br />

cases which were identified in the new syndrome to understand clearly about<br />

the pathology <strong>of</strong> coloboma <strong>of</strong> the eyelid.<br />

Methods: Two cases <strong>of</strong> coloboma <strong>of</strong> the eyelid, one boy and one girl, the age<br />

<strong>of</strong> 8 and 9, are living in Tay Nguyen and South Vietnam. Both cases were<br />

examined systematically and performed paraclinic tests.<br />

Results: Both cases had manifestations:coloboma <strong>of</strong> the upper eyelid,<br />

choristoma on the cornea and conjunctiva, incomplete alopecia, cutaneous<br />

nevoid lesions. Besides, one case had microphthalmia. The findings <strong>of</strong><br />

the syndrome involved disturbances <strong>of</strong> development <strong>of</strong> the embryo and<br />

differentiated process <strong>of</strong> cranio-facial mass, they mixed embryonic dysgenesis<br />

syndrome which were classified as the First Branchial Arch Anomalies.<br />

Conclusions: Coloboma <strong>of</strong> the eyelid combined with choristoma may encounter<br />

not only in the oculo-fronto-cutaneous syndrome which described by the<br />

author Nguyen Duy Tan in 1973, but also in the clinical formes <strong>of</strong> coloboma <strong>of</strong><br />

the eyelid associated with systematic disorders.<br />

PO-PED-02<br />

No suture lensectomy in the pediatric population<br />

O› Halloran Henry (1) , Fikhman Michael (1)<br />

1. Rady Children›s Hospital<br />

Objective; To look at the use <strong>of</strong> no suture Lensectomy in the pediatric<br />

population. Methods; a retrospective <strong>of</strong> 10 years <strong>of</strong> no suture lensectomy in<br />

our pediatric Patient Population. Results; We find the no suture teqhnique to<br />

se safe and effective in children. Conclusion; we recommend the use <strong>of</strong> the no<br />

suture technique in pediatric patients.<br />

PO-PED-03<br />

Surgery as primary intervention in glaucoma in the pediatric<br />

population<br />

O› Halloran Henry (1) , Fikhman Michael (1)<br />

1. Rady Children›s Hospital<br />

Objective; To determine if surgery is the best primary intervention for children<br />

with glaucoma methods; a chart review <strong>of</strong> our pediatric glaucoma patients<br />

over the past 5 years who were treated primarily either medically or surgically.<br />

results; we found surgery to be a safe and effective primary treatment choice.<br />

Conclusion; we recommend consideration <strong>of</strong> surgery rather than topical<br />

medications as a primary treatment in the pediatric glaucoma population.<br />

584<br />

PO-PED-04<br />

Comparative study <strong>of</strong> bilateral lateral rectus recession versus OU<br />

medial rectus tucking or OU medial rectus resection in the treatment<br />

<strong>of</strong> intermittent exotropia<br />

diab mohamed (1)<br />

1. Pediatric and Strabismus<br />

Purpose: To compare between bilateral lateral rectus recession versus OU<br />

medial rectus tucking OU medial rectus resection in the treatment <strong>of</strong> intermittent<br />

exotropia as regards surgical outcome in different age group and degree <strong>of</strong><br />

the strabismus Patients and methods 63 cases <strong>of</strong> intermittent exotropia were<br />

divided into three equal surgical groups. Group A included cases whom bilateral<br />

lateral rectus recession was done. Group B included cases in which bilateral<br />

medial rectus tucking was done Group C included cases whom bilateral medial<br />

rectus resection was proceeded<br />

Results: When comparing the success rates <strong>of</strong> group A, B and C as regard the<br />

grade <strong>of</strong> deviation measured pre operatively we can decide bilateral medial<br />

rectus recession or tucking were more effective in larger angle <strong>of</strong> deviation.<br />

As regard age group we can decide bilateral medial rectus recession or<br />

tucking were more effective in older age group but can induce overcorrection<br />

in younger age group<br />

Conclusion: medial rectus recession or tucking is more safe and effective<br />

procedure in the treatment <strong>of</strong> intermittent exotropia especially among large<br />

angles <strong>of</strong> deviation in older patients<br />

PO-PED-05<br />

Association <strong>of</strong> Complement Factor H and ARMS2 Genotypes with<br />

subtypes <strong>of</strong> Polypoidal Choroidal Vasculopathy<br />

Tanaka Koji (1) , Nakayama Tomohiro (1) , Yuzawa Mitsuko (1)<br />

1. Division <strong>of</strong> Ophthalmology Surugadai-Hospital Nihon University<br />

Purpose: To clarify whether complement factor H (CFH) and age-related<br />

maculopathy susceptibility 2 (ARMS2) genotypes are associated with subtypes<br />

<strong>of</strong> polypoidal choroidal vasculopathy (PCV), such as polypoidal choroidal<br />

neovascularization (CNV) and typical PCV.<br />

Methods: We categorized 287 patients as having polypoidal CNV (85 patients)<br />

or typical PCV (202 patients) based on indocyanine green angiographic<br />

findings. 277 subjects without age-related macular degeneration (AMD) served<br />

as controls. I62V (rs800292) in the CFH gene and A69S (rs10490924) in the<br />

ARMS2 gene were genotyped, and case-control studies were performed in<br />

subjects with these PCV subtypes.<br />

Results: There were significant differences in all distributions <strong>of</strong> rs800292<br />

between the case groups and the controls. Though there were significant<br />

differences in all distributions <strong>of</strong> rs10490924 between the polypoidal CNV and<br />

control groups, there was no difference between the typical PCV and control<br />

groups. Logistic regression analysis with adjustment for confounding factors<br />

showed the distributions <strong>of</strong> rs10490924 to differ highly significantly between<br />

the controls and polypoidal CNV cases (p=2.1~10-10).<br />

Conclusions: PCV might be genetically divided into polypoidal CNV and typical<br />

PCV. The rs10490924 variant <strong>of</strong> the ARMS2 gene was shown to be associated<br />

with polypoidal CNV. Typical PCV was not associated with this variant.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!