- About this Journal ·
- Abstracting and Indexing ·
- Advance Access ·
- Aims and Scope ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
Case Reports in Medicine
Volume 2014 (2014), Article ID 506804, 5 pages
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.
- W. C. Grabb, “The first and second branchial arch syndrome,” Plastic and Reconstructive Surgery, vol. 36, no. 5, pp. 485–508, 1965.
- 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.
- R. J. Gorlin, “Oculoauriculovertebral dysplasia,” The Journal of Pediatrics, vol. 63, no. 5, pp. 991–999, 1963.
- 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.
- J. M. Opitz and G. C. Faith, “Visceral anomalies in an infant with the Goldenhar syndrome,” Birth Defects, vol. 5, pp. 104–105, 1969.
- 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.
- Japanese Society of Pediaric Dentistry, “A study on the cephalometric standards of Japanese children,” Pediatric Dental Journal, vol. 33, pp. 659–696, 1995.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- D.-J. Kleinjan and V. Van Heyningen, “Position effect in human genetic disease,” Human Molecular Genetics, vol. 7, no. 10, pp. 1611–1618, 1998.
- 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.
- 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.
- 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.
- 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.