Bilateral Persistent Pupillary Membrane with Tetralogy of Fallot: A Case Report and Review of the Literature
Author(s) -
Ahmet Altun,
Sevda Aydın Kurna,
Ercüment Bozkurt,
Gürkan Erdoğan,
Gulengul Altun,
Osman Okan Olcaysü,
Suat Fazıl Akı
Publication year - 2014
Publication title -
case reports in ophthalmological medicine
Language(s) - English
Resource type - Journals
eISSN - 2090-6722
pISSN - 2090-6730
DOI - 10.1155/2014/581273
Subject(s) - medicine , tetralogy of fallot , photophobia , visual acuity , ophthalmology , pinhole (optics) , pupil , optometry , cardiology , psychology , heart disease , neuroscience , physics , optics
Case Report . A 15-year-old boy presented to the Fatih Sultan Mehmet Education and Research Hospital with the complain of bilateral vision blurring associated with severe glare and photophobia. On ophthalmological examination, uncorrected visual acuity was 20/200 in the right eye and 20/100 in the left eye, and there was no improvement with pinhole testing. The slit-lamp examination showed persistent pupillary membranes (PPM) in both eyes. According to the history obtained from his parents, he had received cardiac surgery for tetralogy of Fallot (TOF) 8 years ago. Conclusion . This patient is unique because this is the first reported case of bilateral PPM with congenital heart anomaly in the literature. Bilaterality of the eye anomaly strengthens the possibility of an uncommon association between PPM and TOF, rather than local failure in embryonic development.
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