Article Menu

Export Article

More by Authors Links

Article Data

  • Views 2017
  • Dowloads 123

Case Reports

Open Access

Alternative rehabilitation treatment for a patient with ectodermal dysplasia

  • Daniella Della Valle1,*,
  • Ana Beatriz Alonso Chevitarese2
  • Lucianne Cople Maia3
  • Joao Alfredo Farinhas3

1Av. General Felicíssimo Cardoso, 835, Bl. 2/811, Zip Code: 22631-360, Barra da Tijuca, Rio de Janeiro, RJ, Brazil

2Rua Conde de Bonfim, 573/804,Tijuca, Rio de Janeiro, RJ, Brazil

3Av. Brigadeiro Trompowsy s/nº, Cidade Universitária Ilha do Governador, Rio de Janeiro, RJ, Brazil.

DOI: 10.17796/jcpd.28.2.55021560w701h2r2 Vol.28,Issue 2,April 2004 pp.103-106

Published: 01 April 2004

PDF (99.31 kB) View Full-text

Abstract

The ectodermal dysplasia constitutes a group of hereditary disorders whose clinical manifestations can be defects in ectodermal structures. The hypohidrotic and anihidrotic are commonly types of ectodermal dysplasia.The main characteristics are dental anomalies, hypotrichosis and hypohidrosis.The oral rehabilitation of this patients is important for better social living, self esteem and oral function. This paper had as objective to relate and discuss a case of anihidrotic ectodermal dysplasia, describing the positive influence of an alternative rehabilitation treatment.

Cite and Share

Daniella Della Valle,Ana Beatriz Alonso Chevitarese,Lucianne Cople Maia,Joao Alfredo Farinhas. Alternative rehabilitation treatment for a patient with ectodermal dysplasia. Journal of Clinical Pediatric Dentistry. 2004. 28(2);103-106.

URL:

https://www.jjocpd.com/articles/10.17796/jcpd.28.2.55021560w701h2r2

References

1. Boj JR, Duran von Arx J, Cortada M, Jimenez A, Golobart J. Dentures for a 3-yr-old child with ectodermal dysplasia: case report. Am J Dent 6: 165-7, 1993.

2. Abadi B, Herren C. Clinical treatment of ectodermal dysplasia: a case report. Quintessence Int 32: 743-5, 2001.

3. Awwaad S, Essany ME. Hereditary anihidrotic ectodermal dysplasia. Arch Pediatr 77: 196-502, 1960.

4. Familusi JB, Jaiyesimi F, Ojo CO, Attah EB. Hereditary anihypohidrotic ectodermal dysplasia. Studies in a Nigerian family. Arch Dis Child 50: 642-7, 1975.

5. Neville BW. Oral and maxillofacial pathology. Philadelphia, WB Saunders Company, 1995.

6. Vierucci S, Baccetti T, Tollaro I. Dental and craniofacial findings in hypohypohidrotic ectodermal dysplasia during the primary dentition phase. J Clin Ped Dent 18: 291-7, 1994.

7. Clarke A, Phillips DI, Brown R, Harper PS. Clinical aspects of X-linked hypohypohidrotic ectodermal dysplasia. Arch Dis Child 62: 989-96, 1987.

8. Gorlin RJ. Syndromes of the head and neck. 3rd Ed. New York, Oxford, pp 451-6, 1990.

9. Capitanio MA, Chen JT, Arey JB, Kirkpatrick JA. Congenital anihidrotic ectodermal dysplasia. Am J Roentgenol 103: 168-72, 1968.

10. Usulu T, Alacam A, Iscan TN, Ucuncu N. Relation of ectodermal dysplasia and hypodontia. J Clin Ped Dent 15: 46-50, 1990.

11. Kupietzky A, Houpt M. Hypohidrotic ectodermal dysplasia: characteristics and treatment. Quintessence Int 26: 285-91, 1995.

12. Freire-Maia N. Ectodermal dysplasias. Hum Hered 21: 309-12, 1971.

13. Anil K. Anodontia associated with hypohidrotic ectodermal dysplasia. J Pierre Fauchard Acad 6: 55-9, 1992.

14. Ektrand K, Thompsson N. Ectodermal dysplasia with partial anodontia: prosthetic treatment with implant fixed prosthesis. J Dent Child 55: 282-4, 1988.

15. Guckes AD, McCarthy GR, Brahim J. Use of endosseous implants in a 3-year-old child with ectodermal dysplasia: case report and 5-year follow-up. Pediatr Dent 19: 282-5, 1997.

Submission Turnaround Time

Top