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Hassanpour K, Nourinia R, Behnaz N, Azarmina M, Jalali S, Roshandel D. Bilateral Keratoconus in a Patient with Isolated Foveal Hypoplasia. JOVR [Internet]. 2020Apr.6 [cited 2024Jul.17];15(2):256–258. Available from: https://knepublishing.com/index.php/JOVR/article/view/6745

https://doi.org/10.18502/jovr.v15i2.6745

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authors

  • Kiana Hassanpour

    Kiana Hassanpour

    Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  • Ramin Nourinia

    Ramin Nourinia

    Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  • Nazanin Behnaz

    Nazanin Behnaz

    Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  • Mohsen Azarmina

    Mohsen Azarmina

    Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  • Setareh Jalali

    Setareh Jalali

    Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  • Danial Roshandel

    Danial Roshandel

    Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    https://orcid.org/0000-0002-6716-6406

Published Date

  • Apr 6, 2020
This journal is publishing all the articles under Creative Commons Attribution License CC BY 4.0.

Bilateral Keratoconus in a Patient with Isolated Foveal Hypoplasia

Journal of Ophthalmic and Vision Research (JOVR) / April–June 2020, Volume 15, Issue 2 / Pages 256–258

Abstract

This is a Photo Essay and does not have an abstract.

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References
1. Kwon JY, Marmor M, Kodsi SR. Clinical characteristics of isolated foveal hypoplasia: a case series. J Am Assoc Pediatr Ophthalmol Strabismus 2016;20:e36.

2. Weed KH, MacEwen CJ, Giles T, Low J, McGhee CN. The Dundee University Scottish Keratoconus study: demographics, corneal signs, associated diseases, and eye rubbing. Eye 2008;22:534.

3. Vincent AL, Jordan C, Sheck L, Niederer R, Patel DV, McGhee CN. Screening the visual system homeobox 1 gene in keratoconus and posterior polymorphous dystrophy cohorts identifies a novel variant. Mol Vis 2013;19:852.