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Retina Arter Tıkanıklıkları ve Tedavisi...
Santral Retinal Ven Tıkanıklığı Güncel Tedavisi...
Central Retinal Artery Occlusion As the Cause of Unilateral Concentric Narrowing of Visual Field and Presence of Cilioretinal Artery...
Bilateral Optic Disc Drusen
Vascular Endothelial Growth Factor and Anti VEGF Agents...
Central Retinal Artery Occlusion As the Cause of Unilateral Concentric Narrowing of Visual Field and Presence of Cilioretinal Artery...
Retina Arter Tıkanıklıkları ve Tedavisi...
Morning Glory Syndrome Associated with Retinochoroidal Coloboma...
Santral Retinal Ven Tıkanıklığı Güncel Tedavisi...
Bilateral Optic Disc Drusen
PureSee Kesintisiz Yüksek Kalitede Görüş
Retina-Vitreous 2012 , Vol 20 , Num 4
Turkish Abstract Abstract Article PDF Similar Articles Mail to Author
The Distribution of Congenital Ocular Malformations in Newborn Ocular Screening
İkbal Seza PETRİÇLİ1, Zuhal ÖZEN TUNAY2, Özdemir ÖZDEMİR3
M.D., Zekai Tahir Burak Women’s Healt Training and Research Hospital, Eye Clinic, Ankara/TURKEY Purpose: To examine the distribution of congenital ocular anomalies in newborn screening and to emphasize the importance of directing families for necessary treatment, rehabilitation programs and genetic counseling.

Materials and Methods: 12844 eyes of 6422 newborns who were born in Zekai Tahir Burak Women's Health Education and Research Hospital between January 2006 and December 2011 were examined. 6097 newborns were scanned for retinopathy of prematurity (ROP) and 325 newborns were consulted for eye examination from the neonatology department. Our study is a descriptive study based on records.

Results: Congenital eye anomalies were detected in 101 eyes (7.86%). Of these 101 eyes, 57 eyes were diagnosed in consulted babies for anomaly screening and 44 eyes were diagnosed during ROP screening. Anterior segment anomalies were detected in 52 eyes (51.4%), posterior segment anomalies were determined in 19 eyes (18.8%) and both the anterior and posterior segment anomalies were found in 30 eyes (29.7%). The most frequently detected anomaly was coloboma (28.7%) and 3 eyelid, 10 iris, 4 chorioretinal, 6 iris-chorioretinal, 3 optic disk, and 3 iris-chorioretinal-optic disc coloboma were observed. In 12194 eyes scanned for ROP, the anomaly rate was 3.32% and the most frequently anomaly was coloboma (1.06%). In 650 eyes examined for anomaly screening, the anomaly rate was 8.76% and the most common anomaly was coloboma (2.0%).

Conclusion: The most common congenital eye anomalies observed in this study were coloboma and microphtalmia. Detailed systemic and eye examination is essential in anomalous newborns for early diagnosis and treatment of associated lesions. Keywords : Coloboma, congenital eye anomaly, neonatal, retinopathy of prematurity

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