Journals / BEYOGLU EYE JOURNAL / 2019 / Cilt: 4 - Sayı: 1

Orbital Compartment Syndrome

Pages
1–4
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Presented here is a brief summary of OCS in order to call attention to this condition.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Orbital compartment syndrome (OCS) is a true ophthalmological emergency.
📊
Key Findings & Data:It develops as a result of an acute rise in intra-orbital pressure, and if not treated immediately, damage to the optic disc and retina will lead to irreversible vision loss.
💡
Conclusion & Impact:Presented here is a brief summary of OCS in order to call attention to this condition.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Orbital compartment syndrome (OCS) is a true ophthalmological emergency. It develops as a result of an acute rise in intra-orbital pressure, and if not treated immediately, damage to the optic disc and retina will lead to irreversible vision loss. Thus, immediate diagnosis and management are vital to preserve vision. Presented here is a brief summary of OCS in order to call attention to this condition.

🔖

Cite This Article

TURGUT, B., KARANFİL, F. Ç., TURGUT, F. A. (2019). Orbital Compartment Syndrome. BEYOGLU EYE JOURNAL, Cilt: 4 - Sayı: 1, 1–4. https://ajindex.com/articles/143172

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (7)

  1. Wajntal A, Koiffmann CP, Mendonça BB, Epps-Quaglia D, Sotto MN, Rati PB, et al. GAPO syndrome (McKusick 23074)--a con-nective tissue disorder: report on two affected sibs and on the pathologic findings in the older. Am J Med Genet 1990;37:213– 23. Meguid NA, Afifi HH, Ramzy MI, Hindawy A, Temtamy SA. GAPO syndrome: first Egyptian case with ultrastructural changes in the gingiva. Clin Genet 1997;52:110–5.
  2. Ilker SS, Oztürk F, Kurt E, Temel M, Gül D, Sayli BS. Ophthalmic findings in GAPO syndrome. Jpn J Ophthalmol 1999;43:48–52.
  3. Bacon W, Hall RK, Roset JP, Boukari A, Tenenbaum H, Walter B. GAPO syndrome: a new case of this rare syndrome and a re-view of the relative importance of different phenotypic features in diagnosis. J Craniofac Genet Dev Biol 1999;19:189–200.
  4. Touzri RA, Goucha S, Kriaa L, Beltaif O, Fazaa B, El Andol-si H, et al. Ocular manifestation in GAPO syndrome. Report of the first tunisian case. [Article in French]. J Fr Ophtalmol 2003;26:1067–70.
  5. Bozkurt B, Yildirim MS, Okka M, Bitirgen G. GAPO syndrome: four new patients with congenital glaucoma and myelinated ret-inal nerve fiber layer. Am J Med Genet A 2013;161A:829–34.
  6. Goucha S, Fazaa B, Ezzine N, Jaber K, Elandaloussi H, Abid R, et al. GAPO syndrome. [Article in French]. Ann Dermatol Ve-nereol 2000;127:501–4.
  7. Costa VP, Smith M, Spaeth GL, Gandham S, Markovitz B. Loss of visual acuity after trabeculectomy. Ophthalmology 1993;100:599–612.