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Case Reports in Medicine
Volume 2014 (2014), Article ID 506804, 5 pages
http://dx.doi.org/10.1155/2014/506804
Case Report

Clinical Approach to a Suspected Case of First Branchial Arch Syndrome

1Section of Pediatric Dentistry, Division of Oral Health, Growth and Development, Faculty of Dental Science, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan
2Department of Pediatric Dentistry, Kyushu University Hospital, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan

Received 24 August 2013; Accepted 28 November 2013; Published 12 January 2014

Academic Editor: Luis García-Marcos

Copyright © 2014 Noboru Yamaguchi 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. W. C. Grabb, “The first and second branchial arch syndrome,” Plastic and Reconstructive Surgery, vol. 36, no. 5, pp. 485–508, 1965. View at Scopus
  2. R. C. M. Hennekam, I. D. Krantz, and J. E. Allanson, “Branchial arch and oro-acral disorders,” in Gorlin’s Syndromes of the Head and Neck, pp. 879–887, Oxford University Press, New York, NY, USA, 5th edition, 2010.
  3. R. J. Gorlin, “Oculoauriculovertebral dysplasia,” The Journal of Pediatrics, vol. 63, no. 5, pp. 991–999, 1963. View at Scopus
  4. M. M. Cohen Jr., “Variability versus “incidental findings” in the first and second branchial arch syndrome: unilateral variants with anophthalmia,” Birth Defects Original Article Series, vol. 7, no. 7, pp. 103–108, 1971. View at Scopus
  5. J. M. Opitz and G. C. Faith, “Visceral anomalies in an infant with the Goldenhar syndrome,” Birth Defects, vol. 5, pp. 104–105, 1969.
  6. D. Poswillo, “The pathogenesis of the first and second branchial arch syndrome,” Oral Surgery, Oral Medicine, Oral Pathology, vol. 35, no. 3, pp. 302–328, 1973. View at Scopus
  7. Japanese Society of Pediaric Dentistry, “A study on the cephalometric standards of Japanese children,” Pediatric Dental Journal, vol. 33, pp. 659–696, 1995.
  8. Y. Sasaki, K. Satoh, H. Hayasaki, S. Fukumoto, T. Fujiwara, and K. Nonaka, “The P561T polymorphism of the growth hormone receptor gene has an inhibitory effect on mandibular growth in young children,” European Journal of Orthodontics, vol. 31, no. 5, pp. 536–541, 2009. View at Publisher · View at Google Scholar · View at Scopus
  9. D. Kelberman, J. Tyson, D. Chandler et al., “Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome,” Human Genetics, vol. 109, no. 6, pp. 638–645, 2001. View at Publisher · View at Google Scholar · View at Scopus
  10. S. Tobiume, K. Fujisawa, H. Nakanishi, et al., “A case of first and second branchial arch syndrome in a patient whose profile and occlusion improved in response to orthognatic surgery,” Journal of Oral and Maxillofacial Surgery, vol. 46, pp. 96–98, 2000.
  11. G. Yamada, A. Mansouri, M. Torres et al., “Targeted mutation of the murine goosecoid gene results in craniofacial defects and neonatal death,” Development, vol. 121, no. 9, pp. 2917–2922, 1995. View at Scopus
  12. G. Yamada, K. Ueno, S. Nakamura et al., “Nasal and pharyngeal abnormalities caused by the mouse goosecoid gene mutation,” Biochemical and Biophysical Research Communications, vol. 233, no. 1, pp. 161–165, 1997. View at Publisher · View at Google Scholar · View at Scopus
  13. M. Blum, E. M. De Robertis, T. Kojis et al., “Molecular cloning of the human homeobox gene goosecoid (GSC) and mapping of the gene to human chromosome 14q32.1,” Genomics, vol. 21, no. 2, pp. 388–393, 1994. View at Publisher · View at Google Scholar · View at Scopus
  14. D.-J. Kleinjan and V. Van Heyningen, “Position effect in human genetic disease,” Human Molecular Genetics, vol. 7, no. 10, pp. 1611–1618, 1998. View at Publisher · View at Google Scholar · View at Scopus
  15. A. Trumpp, M. J. Depew, J. L. R. Rubenstein, J. M. Bishop, and G. R. Martin, “Cre-mediated gene inactivation demonstrates that FGF8 is required for cell survival and patterning of the first branchial arch,” Genes and Development, vol. 13, no. 23, pp. 3136–3148, 1999. View at Publisher · View at Google Scholar · View at Scopus
  16. J. Zhang, S. Hagopian-Donaldson, G. Serbedzija et al., “Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2,” Nature, vol. 381, no. 6579, pp. 238–241, 1996. View at Publisher · View at Google Scholar · View at Scopus
  17. Y. Kurihara, H. Kurihara, H. Suzuki et al., “Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1,” Nature, vol. 368, no. 6473, pp. 703–710, 1994. View at Publisher · View at Google Scholar · View at Scopus
  18. K. Nonaka, T. Inoguchi, Y. Tachikawa, et al., “Oro-facial findings in a patient with oculo-dento-digital syndrome,” Japanese Journal of Pediatrics, vol. 32, pp. 926–933, 1994.