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   Table of Contents      
OPHTHALMIC IMAGE
Year : 2020  |  Volume : 68  |  Issue : 8  |  Page : 1668

Ultra-widefield noncontact imaging of bilateral congenital retinal fold


1 Department of Vitreoretina Services, Disha Eye Hospitals, Kolkata, West Bengal, India
2 Department of Ocular Pathology, Uveitis and Neuro-Ophthalmology Services, Sri Sankaradeva Nethralaya, Guwahati, Assam, India

Date of Web Publication24-Jul-2020

Correspondence Address:
Dr. Debdulal Chakraborty
Department of Vitreo.retina Services, Disha Eye Hospitals, Ghosh Para Road, Barrackpore, Kolkata - 700 120, West Bengal
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijo.IJO_2305_19

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How to cite this article:
Chakraborty D, Das D. Ultra-widefield noncontact imaging of bilateral congenital retinal fold. Indian J Ophthalmol 2020;68:1668

How to cite this URL:
Chakraborty D, Das D. Ultra-widefield noncontact imaging of bilateral congenital retinal fold. Indian J Ophthalmol [serial online] 2020 [cited 2020 Aug 12];68:1668. Available from: http://www.ijo.in/text.asp?2020/68/8/1668/290438



A 20-year old presented with visual acuity 20/200 (both eye). Anterior segment findings and intraocular pressures were unremarkable. Fundus examination revealed bilateral retinal fold extending from disc to inferotemporal periphery, with retinal blood vessels on the fold [Figure 1]. Fovea was not discernible. Pigmentary change was noted along the fold, more toward periphery.
Figure 1: Optos widefield image of right eye (a) and left eye (b) showing bilateral retinal fold (red star) with peripheral retina showing white without pressure in left eye (red triangle)

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First described by Mann,[1] congenital retinal folds (CRF) extend temporally in 92.5%, have poor vision, and 75% are unilateral.[2],[3] 30% eyes may develop devastating posterior segment complications.[2],[3] Common causes of CRF are retinopathy of prematurity (ROP), familial exudative vitreoretinopathy (FEVR), Norrie disease, etc.[1],[2],[3],[4] Early diagnosis and intervention are essential to preserve useful vision.[3],[4] Noncontact ultra-widefield retinal imaging (Optos) of bilateral CRF [Figure 1] has never been described in the scientific literature previously and may be useful in the follow-up of those eyes.

Acknowledgement

Mr. Sudip Ghosh, Ophthalmic photographer.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Van Nouhuys CE. Congenital retinal fold as a sign of dominant exudative vitreoretinopathy. Albrecht von Graefes Arch Klin Ophthalmol 1981;217:55-67.  Back to cited text no. 1
    
2.
Nishina S, Suzuki Y, Yokoi T, Kobayashi Y, Noda E, Azuma N. Clinical features of congenital retinal folds. Am J Ophthalmol 2012;153:81-7.e1.  Back to cited text no. 2
    
3.
Suzuki Y, Nishina S, Hiraoka M, Yokoi T, Azuma N. Congenital rotated macula with good vision and binocular function. Jpn J Ophthalmol 2009;53:452-4.  Back to cited text no. 3
    
4.
Warburg M. Hydrocephaly, congenital retinal nonattachment and congenital falciform fold. Am J Ophthalmol 1978;85:88-94.  Back to cited text no. 4
    


    Figures

  [Figure 1]



 

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