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Enamel Pit Defects and Taurodontism in a Patient with Ring Chromosome 14 and 47,XXX

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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.
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Keywords: 47,XXX; DEVELOPMENTAL ANOMALIES; RING CHROMOSOME 14

Document Type: Case Report

Affiliations: 1: Associate professor and chair, Department of Pediatric Dentistry, Louisiana State University Health Sciences Center School of Dentistry, New Orleans, La., USA;, Email: jtown2@lsuhsc.edu 2: Dentist in private practice, Hammond, La., USA 3: Professor, Department of Pediatrics, Division of Genetics and Metabolism, University of Texas Southwestern Medical Center, Dallas, Texas, USA

Publication date: 2017-01-01

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  • Acquired after the merger between the American Society of Dentistry for Children and the American Academy of Pediatric Dentistry in 2002, the Journal of Dentistry for Children (JDC) is an internationally renowned journal whose publishing dates back to 1934. Published three times a year, JDC promotes the practice, education and research specifically related to the specialty of pediatric dentistry. It covers a wide range of topics related to the clinical care of children, from clinical techniques of daily importance to the practitioner, to studies on child behavior and growth and development. JDC also provides information on the physical, psychological and emotional conditions of children as they relate to and affect their dental health.
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