International Journal of Clinical Pediatric Dentistry

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VOLUME 4 , ISSUE 3 ( September-December, 2011 ) > List of Articles


Ectodermal Dysplasia: A Case Report

Vinay K Srivastava

Keywords : Midface hypoplasia, Double lip, Partial anodontia

Citation Information : Srivastava VK. Ectodermal Dysplasia: A Case Report. Int J Clin Pediatr Dent 2011; 4 (3):269-270.

DOI: 10.5005/jp-journals-10005-1124

License: CC BY-NC 4.0

Published Online: 01-12-2014

Copyright Statement:  Copyright © 2011; The Author(s).


Ectodermal dysplasia is a hereditary disease characterized by dysplasia of tissues of ectodermal origin. The incidence of ectodermal dysplasia is rare (1 in 100,000 birth). This case report discusses the features, classification and prosthetic treatment plan (upper partial denture and lower complete denture for upper partial and lower complete edentulous arches respectively). This treatment plan would be able to provide psychological and functional boost to the sufferer.

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  1. Pinheiro M, Freire-Maia N. Ectodermal dysplasia: A clinical classification and a casual review. Am J Med Genet Nov 1, 1994;53(2):153-62.
  2. Smith FJ, Jonkman MF, Van Goor, et al. A mutation in human keratin K6b produces a phenocopy of the K17 disorders pachyonychia type 2. Hum Mol Genet Jul 1998;7(7):1143-48.
  3. Mc Lean WH, et al. Keratine 16 and keratine 17 mutations causes pachyonychia congenital. Nat Genet Mar 1995;9(3): 273-78.
  4. Boden PE, Haley JL, et al. Mutation of a type II keratine gene (K6a) in pachyonychia congenital. Nat Genet Jul 1995;10(3): 363-65.
  5. Kere J, Srivastava AK, Montonen O, et al. X-linked anhidrotic (hypohydrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet Aug 1996;13(4):409-16.
  6. Monreal AW, et al. Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutation (published erratum appears in Am J Hum Genet Oct 1998;63(4):1253-55). Am J Hum Genet Aug 1998;63(2):380-89.
  7. Lamartine J, Munhoz, et al. Mutation in GJB6 cause hidrotic ectodermal dysplasia. Nat Genet Oct 2000;26(2):142-44.
  8. Moreal AW, Ferguson BM, Headon, et al. Mutation in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nat Genet Aug 1999;22(4): 366-69.
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