Literature DB >> 292959

Amelogenesis imperfecta with taurodontism.

J Congleton, E J Burkes.   

Abstract

Reports of families having a combination of amelogenesis imperfecta and taurodontism are limited. This study of members of three families shows that the combination is inherited as an autosomal dominant trait. In each of the patients examined, neither condition was seen without the other. The enamel was rough and dysplastic and varied in color from white to yellow. Radiographically, taurodontism was present in the deciduous and permanent dentitions. The pulp chambers of the incisor teeth were larger than is usually seen at all ages. All patients had normal-appearing hair, fingernails, and bones. The distinction between amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome is discussed.

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Year:  1979        PMID: 292959     DOI: 10.1016/0030-4220(79)90301-3

Source DB:  PubMed          Journal:  Oral Surg Oral Med Oral Pathol        ISSN: 0030-4220


  3 in total

Review 1.  Taurodontism, an isolated trait associated with syndromes and X-chromosomal aneuploidy.

Authors:  M T Jaspers; C J Witkop
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025

2.  Amelogenesis imperfecta and generalized gingival overgrowth resembling hereditary gingival fibromatosis in siblings: a case report.

Authors:  Emre Yaprak; Meryem Gülce Subaşı; Mustafa Avunduk; Filiz Aykent
Journal:  Case Rep Dent       Date:  2012-10-09

3.  Tricho-dento-osseous syndrome: diagnosis and dental management.

Authors:  Ola B Al-Batayneh
Journal:  Int J Dent       Date:  2012-08-27
  3 in total

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