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Case Reports in Ophthalmological Medicine
Volume 2015, Article ID 626027, 4 pages
Case Report

A Case of Goldenhar Syndrome Associated with a New Retinal Presentation: Exudative Vitelliform Maculopathy

Ophthalmology, Department of Neuroscience, Polytechnic University of Marche, 60039 Ancona, Italy

Received 11 March 2015; Accepted 23 April 2015

Academic Editor: Shigeki Machida

Copyright © 2015 Claudia Bruè 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. J. K. Sharma, S. K. Pippal, S. K. Raghuvanshi, and A. Shitij, “Goldenhar-Gorlin's syndrome: a case report,” Indian Journal of Otolaryngology and Head and Neck Surgery, vol. 58, no. 1, pp. 97–101, 2006. View at Google Scholar · View at Scopus
  2. H. Martelli Jr., R. T. de Miranda, C. M. Fernandes et al., “Goldenhar syndrome: clinical features with orofacial emphasis,” Journal of Applied Oral Science, vol. 18, no. 6, pp. 646–649, 2010. View at Publisher · View at Google Scholar · View at Scopus
  3. B. R. Rollnick, C. I. Kaye, K. Nagatoshi, W. Hauck, and A. O. Martin, “Oculoauriculovertebral dysplasia and variants: phenotypic characteristics of 294 patients,” American Journal of Medical Genetics, vol. 26, no. 2, pp. 361–375, 1986. View at Google Scholar · View at Scopus
  4. S. De Golovine, S. Wu, J. V. Hunter, and W. T. Sheater, “Goldenhar syndrome: a cause of secondary immunodeficiency?” Allergy, Asthma & Clinical Immunology, vol. 8, pp. 10–15, 2012. View at Google Scholar
  5. M. Goldenhar, “Associations malformatives de l'oeil et l'oreille, en particulier le syndrome dermoide épibulbaire-appendices auriculaires-fistula auris congenita et ses relations avec la dysostose mandibulo-faciale,” Journal of Human Genetics, vol. 1, pp. 243–282, 1952. View at Google Scholar
  6. H. S. Sugar, “An unusual example of the oculo-auriculovertebral dysplasia syndrome of Goldenhar,” Journal of Pediatric Ophthalmology, vol. 4, pp. 9–12, 1967. View at Google Scholar
  7. S. Aleksic, G. Budzilovich, R. Reuben et al., “Congenital trigeminal neuropathy in oculoauriculovertebral dysplasia-hemifacial microsomia (Goldenhar-Gorlin syndrome),” Journal of Neurology Neurosurgery and Psychiatry, vol. 38, no. 10, pp. 1033–1035, 1975. View at Publisher · View at Google Scholar · View at Scopus
  8. S. Bhallil, I. Benatiya, O. El Abdouni, B. Mahjoubi, and T. Hicham, “Goldenhar syndrome: ocular features,” Bulletin de la Société Belge d'Ophtalmologie, no. 316, pp. 17–19, 2010. View at Google Scholar · View at Scopus
  9. J. Herman and J. M. Opitz, “A dominantly inherited first arch syndrome,” Birth Defects, vol. 5, pp. 110–112, 1969. View at Google Scholar
  10. A. E. Braley and B. E. Spivey, “Hereditary vitelline macular degeneration (possibly of vitelliform origin): a clinical and functional evaluation of a new pedigree with variable expressivity and dominant inheritance,” Transactions of the American Ophthalmological Society, vol. 61, pp. 339–371, 1963. View at Google Scholar