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Case Reports in Dentistry
Volume 2012 (2012), Article ID 281074, 4 pages
http://dx.doi.org/10.1155/2012/281074
Case Report

An Insight into the Genesis of Hypohidrotic Ectodermal Dysplasia in a Case Report

1Department of Oral & Maxillofacial Pathology, I.T.S-CDSR, Muradnagar, Ghaziabad 201206, India
2Department of Oral & Maxillofacial Pathology, Inderprastha Dental College, Sahibabad, Ghaziabad 201010, India
3Department of Prosthodontics, Krishna Dental College, Mohannagar, Ghaziabad 201206, India

Received 26 September 2012; Accepted 27 November 2012

Academic Editors: S. Anil and M. A. Polack

Copyright © 2012 Kiran Kumar 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. A. A. Weech, “Hereditary ectodermal dysplasia (congenital ectodermal defect),” American Journal of Diseases of Children, vol. 37, pp. 766–790, 1929.
  2. L. M. Solomon and E. J. Keuer, “The ectodermal dysplasias. Problems of classification and some newer syndromes,” Archives of Dermatology, vol. 116, no. 11, pp. 1295–1299, 1980. View at Publisher · View at Google Scholar · View at Scopus
  3. D. Perry, Living with x-linked hypohidrotic ectodermal Dysplasia. Ectodermal Dysplasia Society, 108 Charlton Lane, Cheltenham, Glos. GL53 9EA. England.
  4. A. Ul Bari and S. B. Rahman, “Hypohidrotic ectodermal dysplasia: a case report and literature review,” Journal of Pakistan Association of Dermatologists, vol. 17, no. 1, pp. 52–55, 2007. View at Scopus
  5. M. L. Mikkola, “Molecular aspects of hypohidrotic ectodermal dysplasia,” American Journal of Medical Genetics A, vol. 149, no. 9, pp. 2031–2036, 2009. View at Publisher · View at Google Scholar · View at Scopus
  6. D. Berg, D. H. Weingold, K. G. Abson, and E. A. Olsen, “Sweating in ectodermal dysplasia syndromes. A review,” Archives of Dermatology, vol. 126, no. 8, pp. 1075–1079, 1990. View at Publisher · View at Google Scholar · View at Scopus
  7. P. J. Dhanrajani and A. O. Jiffry, “Management of ectodermal dysplasia: a literature review,” Dental Update, vol. 25, no. 2, pp. 73–75, 1998. View at Scopus
  8. M. J. Till and A. P. Marques, “Ectodermal dysplasia: treatment considerations and case reports,” Northwest Dentistry, vol. 71, no. 3, pp. 25–28, 1992. View at Scopus
  9. I. P. Sweeney, J. W. Ferguson, A. A. Heggie, and J. O. Lucas, “Treatment outcomes for adolescent ectodermal dysplasia patients treated with dental implants,” International Journal of Paediatric Dentistry, vol. 15, no. 4, pp. 241–248, 2005. View at Publisher · View at Google Scholar · View at Scopus
  10. G. Varghese and P. Sathyan, “Hypohidrotic ectodermal dysplasia—a case study,” Oral & Maxillofacial Pathology Journal, vol. 2, article 1, 2011.
  11. B. S. Suprabha, “Hereditary ectodermal dysplasia: a case report,” Journal of the Indian Society of Pedodontics and Preventive Dentistry, vol. 20, no. 1, pp. 37–40, 2002. View at Scopus
  12. P. J. M. Crawford, M. J. Aldred, and A. Clarke, “Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia,” Journal of Medical Genetics, vol. 28, no. 3, pp. 181–185, 1991. View at Scopus
  13. S. N. Ramraje, M. Wasnik, and Y. A. Momin, “Anhidrotic ectodermal dysplasia—a report of two cases,” Bombay Hospital Journal, vol. 5, article 12, 2009.
  14. R. Rajendran and B. Sivapathasundaram, Shafer’s Textbook of Oral Pathology, Saunders, Philadelphia, Pa, USA, 5th edition, 1983.
  15. R. M. Shaw, “Prosthetic management of hypohydrotic ectodermal dysplasia with anodontia. Case report,” Australian Dental Journal, vol. 35, no. 2, pp. 113–116, 1990. View at Scopus
  16. S. Vierucci, T. Baccetti, and I. Tollaro, “Dental and craniofacial findings in hypohidrotic ectodermal dysplasia during the primary dentition phase,” The Journal of Clinical Pediatric Dentistry, vol. 18, no. 4, pp. 291–297, 1994. View at Scopus
  17. J. Kere, A. K. Srivastava, O. Montonen et al., “X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein,” Nature Genetics, vol. 13, no. 4, pp. 409–416, 1996. View at Publisher · View at Google Scholar · View at Scopus
  18. F. Munoz, G. Lestringant, V. Sybert et al., “Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X-linked disorder,” American Journal of Human Genetics, vol. 61, no. 1, pp. 94–100, 1997. View at Scopus
  19. J. T. Wright, D. K. Grange, and M. K. Richter, Hypohidrotic Ectodermal Dysplasia, University of Washington, Seattle, Wash, USA, 1993.
  20. D. J. Headon, S. A. Emmal, B. M. Ferguson et al., “Gene defect in ectodermal dysplasia implicates a death domain adapter in development,” Nature, vol. 414, no. 6866, pp. 913–916, 2001. View at Publisher · View at Google Scholar · View at Scopus
  21. S. Cambiaghi, L. Restano, K. Pääkkönen, R. Caputo, and J. Kere, “Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia,” Archives of Dermatology, vol. 136, no. 2, pp. 217–224, 2000. View at Scopus
  22. J. Sharma and G. P. Mamatha, “Hereditary ectodermal dysplasia: diagnostic dilemmas,” Revista de Clínica e Pesquisa Odontológica, vol. 4, no. 1, pp. 35–40, 2008.
  23. A. Kumar, M. T. Eby, S. Sinha, A. Jasmin, and P. M. Chaudhary, “The ectodermal dysplasia receptor activates the nuclear factor-κB, JNK, and cell death pathways and binds to ectodysplasin A,” Journal of Biological Chemistry, vol. 276, no. 4, pp. 2668–2677, 2001. View at Publisher · View at Google Scholar · View at Scopus