Total anodontia in patient with hypohidrotic ectodermal dysplasia. Report of rare case of Christ-Siemens Touraine syndrome.

Amar A. Sholapurkar, Suhas Setty, Keerthilatha M. Pai

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Ectodermal dysplasias are a complex group of genetically determined disorders clinically characterized by congenital alterations of the structures derived from the ectoderm. Even though ectodermal dysplasia with partial anodontia is common, this condition with total anodontia is not. We describe features of hypohidrotic ectodermal dysplasia with complete anodontia in a 6-year-old boy. In order to improve esthetics, speech and mastication, the child was provided with upper and lower complete dentures.

Original languageEnglish
Pages (from-to)36-39
Number of pages4
JournalThe New York state dental journal
Volume77
Issue number1
Publication statusPublished - 01-01-2011

Fingerprint

Anhidrotic Ectodermal Dysplasia 1
Anodontia
Ectodermal Dysplasia
Denture, Complete, Upper
Denture, Complete, Lower
Ectoderm
Mastication
Esthetics

All Science Journal Classification (ASJC) codes

  • Medicine(all)

Cite this

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Total anodontia in patient with hypohidrotic ectodermal dysplasia. Report of rare case of Christ-Siemens Touraine syndrome. / Sholapurkar, Amar A.; Setty, Suhas; Pai, Keerthilatha M.

In: The New York state dental journal, Vol. 77, No. 1, 01.01.2011, p. 36-39.

Research output: Contribution to journalArticle

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