Although congenital ptosis may rarely present with ocular and systemic congenital malformations, ophthalmologists should be alert for coexisting structural defects.
📌 3 Key Takeaways
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Objective & Hypothesis:We report a case with congenital ptosis that is associated with ocular and systemic congenital malformations including mild microphthalmia, microcornea, congenital cataract, iris coloboma, chorioretinal coloboma, pelvic kidney and congenital ventricular septal defect.
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Key Findings & Data:We report a case with congenital ptosis that is associated with ocular and systemic congenital malformations including mild microphthalmia, microcornea, congenital cataract, iris coloboma, chorioretinal coloboma, pelvic kidney and congenital ventricular septal defect.
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Conclusion & Impact:Although congenital ptosis may rarely present with ocular and systemic congenital malformations, ophthalmologists should be alert for coexisting structural defects.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Kolobom · Göz hastalıkları · Doğumsal
Abstract
We report a case with congenital ptosis that is associated with ocular and systemic congenital malformations including mild microphthalmia, microcornea, congenital cataract, iris coloboma, chorioretinal coloboma, pelvic kidney and congenital ventricular septal defect. Although congenital ptosis may rarely present with ocular and systemic congenital malformations, ophthalmologists should be alert for coexisting structural defects.
Özet
Hafif mikroftalmi, mikrokornea, doğumsal katarakt, iris klobomu, korioretinal kolobom, pelvik böbrek ve ventrikül septum hasarını içeren doğumsal göz ve sistemik anomalileri ile birliktelik gösteren doğumsal pitozisli bir olguyu sunmaktayız. Doğumsal pitozis nadiren doğumsal göz ve sistemik anomaliler ile birliktelik göstermesine rağmen, oftalmologlar birlikte bulunan gelişimsel anomaliler konusunda dikkatli olmalıdır
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