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Year : 2022  |  Volume : 2  |  Issue : 1  |  Page : 207-210

Aftermath in Traboulsi syndrome: A case report

1 Senior Consultant in Cornea and Refractive Surgery, Aravind Eye Hospital, Tirunelveli, Tamil Nadu, India
2 Glaucoma Services, Aravind Eye Hospital, Tirunelveli, Tamil Nadu, India
3 Senior Consultant Paediatric and Strabismus Surgery, Aravind Eye Hospital, Tirunelveli, Tamil Nadu, India

Correspondence Address:
Dr. Venugopal Anitha
Aravind Eye Hospital, S.N High Road, Tirunelveli Junction, Tirunelveli - 627 001, Tamil Nadu
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/ijo.IJO_647_21

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To report a long-term (15 years) follow-up of a patient with a rare congenital ophthalmological disorder known as Traboulsi syndrome. It is characterized by ectopia lentis, congenital blebs, and facial dysmorphism. A 25-year-old female was identified with Traboulsi syndrome based on the typical facial, ocular features, and literature evidence. Serial anterior segment optical coherence tomography (ASOCT) and ultrasound biomicroscopy (UBM) were done to document the anterior segment. This case report discusses the clinical aspects of the syndrome such as its long-term sequelae, complications, and management outcomes.

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