Journals / Erciyes Tıp Dergisi / 2010 / Cilt: 32 - Sayı: 1

Duane's retraction syndrome associated with fuchs' uveitis syndrome in the same eye

Duane retraksiyon sendromu ve fuchs üveiti sendromunun aynı gözde beraberliği

Pages
57–60
Publication Date
2022-10-17
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)

These syndromes have no known causal association with each other, and although they occur often, their occurrence together is uncommon.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Duane retraction syndrome is an ocular motility disorder with a number of congenital systemic and eye abnormalities.
📊
Key Findings & Data:Altough, numerous theories concerning the etiology and the pathogenesis of this syndrome are present, still the exact mechanism can not be explained.
💡
Conclusion & Impact:These syndromes have no known causal association with each other, and although they occur often, their occurrence together is uncommon.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Duane retraction syndrome is an ocular motility disorder with a number of congenital systemic and eye abnormalities. Altough, numerous theories concerning the etiology and the pathogenesis of this syndrome are present, still the exact mechanism can not be explained. Fuchs uveitis syndrome is an inflammatory disease of the uvea, thought to be triggered by otoimmunity or some microbial agents. Here , we present a case with two syndromes in the one eye. These syndromes have no known causal association with each other, and although they occur often, their occurrence together is uncommon.

Özet

Duane retraksiyon sendromu, doğumsal birçok sistemik ve göz bozuklukluğun eşlik edebildiği göz hareket bozukluğudur. Hastalığın etyoloji ve patogenezini açıklamaya yönelik birtakım teoriler olsa da gerçek mekanizması tam olarak açıklanamamıştır. Fuchs üveiti sendromu ise otoimmün veya bazı mikrobial ajanların yol açtığı düşünülen uveanin iltihabi bir hastalığıdır. Burada, iki sendromun tek gözde beraberliğini sunuyoruz. Birbirleriyle nedensel ilişkileri bulunmayan bu sendromlar, her ne kadar sık görülseler de beraberlikleri nadirdir.

🔖

Cite This Article

MADEN, A., SAKLAMAZ, A., YILMAZ, S. (2022). Duane's retraction syndrome associated with fuchs' uveitis syndrome in the same eye. Erciyes Tıp Dergisi, Cilt: 32 - Sayı: 1, 57–60. https://ajindex.com/articles/502556

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. OkihiroMM,. Tasaki T, Nakano KK, Bennett BK. Duane syndrome and congenital upper-limb anomalies. Arch Neurol 1977;34:174-179
  2. Pfaffenbach DD, Cross HE, Kearns TP. Congenital anomalies in Duane’s retraction syndrome. Arch Ophthalmol 1972;88:635-639
  3. Hayes A, Costa T, Polomeno RC. The Okihiro syndrome of Duane anomaly, radial ray abnormalities and deafness. Am J Med Genet 1985;22:273-280
  4. Awan KJ. Association of ocular, cervical and cardiac malformations. Ann Ophthalmol 1977; 9:1001-1011
  5. DeRespins PA, Caputo AR, Wagner RS, Guo S. Duane’s retraction syndrome. Surv Ophthalmol 1993; 38:257-288
  6. Fuchs E. Ueber Komplikationen der Heterochromie. Z Augenheilkd 1906;15:191-212. 7) de Visser L, Braakenburg A, Rothova A, de Boer JH. Rubella virus-associated uveitis: clinical manifestations and visual prognosis. Am J Ophthalmol 2008; 146: 292-297
  7. Temtamy SA, Shoukry AS, Ghaly I, et al. The Duane radial dysplasia syndrome: An autosomol dominant disorder. In: New chromosomal and malformation syndromes. New York: Alan R. Liss, Inc. for the National Foundation-March of Dimes. 1975:344-345. SORUNLU YAZIM 9) Guillén-Navarro E, Wallerstein R, Reich E, Zajac L, Ostrer H. Acro-renal-ocular syndrome: expansion of the phenotype. Clin Dysmorphol 1998; 7:243-248
  8. Cullen P, Rodgers CS, Callen DF, et al. Association of familial Duane anomaly and urogenital abnormalities with a bisatellited marker derived from chromosome 22. Am J Med Genet 1993; 47:925-930
  9. Chew CK, Foster P, Hurst JA, Salmon JF. Duane’s retraction syndrome associated with chromosome 4q27- 31 segment deletion. Am J Ophthalmol. 1995;1119: 807-809
  10. Vincent C, Kalatzis V, Compain S et al. A proposed new contiguous gene syndrome on 8q consists of Branchio- Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene. Hum Mol Genet. 1994;3:1859-1866
  11. Ott S, Borchert M, Chung M. et al. Exclusion of candidate genetic loci for Duane retraction syndrome. Am J Ophthalmol. 1999;127:358-360
  12. Jones NP. Fuchs’ heterochromic uveitis: an update. Surv Ophthalmol 1993;37:253-272
  13. Peizeng Y, Wang F, Haoli J, Li B, Chen X, Kijlstra A. Clinical features of Chinese patients with Fuchs’ syndrome. Ophthalmology 2006;113:473-480
  14. Ortega-Larrocea G, Litwak-Sigal S. Astigmatism associated with Fuchs’ heterochromic iridocyclitis. Cornea 2001; 20:366-367.