OCT Findings in A Case With Iris Coloboma and Foveal Hypoplasia

GEDİK C., ŞAHİN L.

Retina-Vitreus, cilt.30, sa.3, ss.291-293, 2021 (Scopus) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 30 Sayı: 3
  • Basım Tarihi: 2021
  • Doi Numarası: 10.37845/ret.vit.2021.30.50
  • Dergi Adı: Retina-Vitreus
  • Derginin Tarandığı İndeksler: Scopus, Academic Search Premier, EMBASE, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.291-293
  • Ondokuz Mayıs Üniversitesi Adresli: Evet

Özet

In foveal hypoplasia there is a continuity of all neurosensory retinal layers in the fovea and loss of foveal pitting. It can be observed in patients with albinism, microphthalmia, aniridi, acromatopsy and premature retinopathy, and rarely in isolated cases. In our case, who presented to our clinic with complaints of deviation in the eyes and decreased distance vision, iris coloboma was present in both eyes on anterior segment examination. On fundus examination, foveal reflex was absent and retinal vessels were observed as slightly tortuos in both eyes. There was no foveal pitting on OCT sections in both eyes. With these findings our case was diagnosed with foveal hypoplasia. The aim of this article is to present the case of iris coloboma and foveal hypoplasia, in whom OCT have an important place in the diagnosis, follow-up and classification. Keywords: Foveal hypoplasia, iris coloboma, OCT.