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Case Reports in Ophthalmological Medicine
Volume 2014, Article ID 312030, 4 pages
http://dx.doi.org/10.1155/2014/312030
Case Report

Unilateral Cataract and Vitreoretinopathy in a Case with Klippel-Trenaunay Syndrome

1Clinic of Ophthalmology, Erzurum Training and Research Hospital, 25240 Erzurum, Turkey
2Clinic of Ophthalmology, Fatih Sultan Mehmet Training and Research Hospital, 34752 Istanbul, Turkey
3Department of Pediatrics, Medical Faculty, Ataturk University, 25240 Erzurum, Turkey
4Department of Medical Genetics, Erzurum Training and Research Hospital, 25240 Erzurum, Turkey
5Department of Radiology, Erzurum Training and Research Hospital, 25240 Erzurum, Turkey

Received 23 April 2014; Accepted 29 May 2014; Published 16 June 2014

Academic Editor: Michele Iester

Copyright © 2014 Osman Okan Olcaysu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. G. G. Kihiczak, J. G. Meine, R. A. Schwartz, and C. K. Janniger, “Klippel-Trenaunay syndrome: a multisystem disorder possibly resulting from a pathogenic gene for vascular and tissue overgrowth,” International Journal of Dermatology, vol. 45, no. 8, pp. 883–890, 2006. View at Publisher · View at Google Scholar · View at Scopus
  2. C. E. U. Oduber, C. M. A. M. van der Horst, and R. C. M. Hennekam, “Klippel-Trenaunay syndrome: diagnostic criteria and hypothesis on etiology,” Annals of Plastic Surgery, vol. 60, no. 2, pp. 217–223, 2008. View at Publisher · View at Google Scholar · View at Scopus
  3. M. Ruggieri, V. Pavone, A. Polizzi, R. Falsaperla, M. Fichera, and P. Pavone, “Klippel-Trenaunay syndrome in a boy with concomitant ipsilateral overgrowth and undergrowth,” American Journal of Medical Genetics A, vol. 164, no. 5, pp. 1262–1267, 2014. View at Google Scholar
  4. L. Dhir and A. G. Quinn, “Persistent fetal vasculature and spontaneous hyphema in a patient with Klippel-Trenaunay-Weber syndrome,” Journal of American Association for Pediatric Ophthalmology and Strabismus, vol. 14, no. 2, pp. 190–192, 2010. View at Publisher · View at Google Scholar · View at Scopus
  5. R. D. Brod, J. A. Shields, C. L. Shields, O. R. Oberkircher, and L. J. Sabol, “Unusual retinal and renal vascular lesions in the Klippel-Trenaunay-Weber syndrome,” Retina, vol. 12, no. 4, pp. 355–358, 1992. View at Google Scholar · View at Scopus
  6. W. V. Good and C. S. Hoyt, “Optic nerve shadow enlargement in the Klippel-Trenaunay-Weber syndrome,” Journal of Pediatric Ophthalmology and Strabismus, vol. 26, no. 6, pp. 288–289, 1989. View at Google Scholar · View at Scopus
  7. T. C. Spoor, J. S. Kennerdell, J. C. Maroon, R. Hepler, and G. Krohel, “Pneumosinus dilatans, Klippel-Trenaunay-Weber syndrome, and progressive visual loss,” Annals of Ophthalmology, vol. 13, no. 1, pp. 105–108, 1981. View at Google Scholar · View at Scopus
  8. S. R. Lambert, C. S. Hoyt, and M. H. Narahara, “Optic nerve hypoplasia,” Survey of Ophthalmology, vol. 32, no. 1, pp. 1–9, 1987. View at Google Scholar · View at Scopus