Enamel pit defects and taurodontism in a patient with ring chromosome 14 and 47,XXX

Janice A. Townsend, Letitia Lacour, Angela E. Scheuerle

Research output: Contribution to journalArticle

Abstract

The purpose of this paper is to describe the clinical findings and management of a case involving a patient with co-occurring ring chromosome 14 syndrome and 47,XXX presenting with enamel pit defects and taurodontism. Ring chromosome 14 syndrome is an unusual condition with uncontrolled seizure disorder as its most significant finding; 47,XXX (trisomy X; triple X) is a more common condition and has characteristic physical and behavioral findings. Neither condition has been associated with enamel pit defects.

Original languageEnglish (US)
Pages (from-to)39-43
Number of pages5
JournalJournal of Dentistry for Children
Volume84
Issue number1
StatePublished - Jan 1 2017

Fingerprint

Dental Enamel
Case Management
Epilepsy
Ring Chromosome 14 Syndrome
Taurodontism
Triple X syndrome

Keywords

  • 47,XXX
  • Developmental anomalies
  • Ring chromosome 14

ASJC Scopus subject areas

  • Medicine(all)
  • Dentistry(all)

Cite this

Enamel pit defects and taurodontism in a patient with ring chromosome 14 and 47,XXX. / Townsend, Janice A.; Lacour, Letitia; Scheuerle, Angela E.

In: Journal of Dentistry for Children, Vol. 84, No. 1, 01.01.2017, p. 39-43.

Research output: Contribution to journalArticle

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