HYPODONTIA: A FAMILIAL CASE REPORT

Authors

  • Gloria Cristina Aránzazu Moya U. Santo Tomás

DOI:

https://doi.org/10.15332/us.v6i2.1810

Keywords:

Hypodontia, Dental abcense, Oligodontia

Abstract

Hypodontia is defined as the ausence of one to six teeth, without considering third molares; it is an event that happens, in the permanent teething, between the 1.6% to 9.6% as much in men as in women. A case of family hypodontia is reported with a pattern of inheritance autosomal recessive, with absence of lateral incisive 22, and second premolar in the four quadrants besides the third molars and microdontia of lateral incisive 12.

Downloads

Download data is not yet available.

Author Biography

Gloria Cristina Aránzazu Moya, U. Santo Tomás

Odontóloga U. Santo Tomás, Especialista en Patología Oral y Medios Diagnósticos U. El Bosque, Docente U. Santo Tomás

References

Hall RK. Congenitally missing teeth – A diagnostic feature in many syndromes of the head and neck. J Int Assoc Dent Child 1983; 14: 69–75

Jorgenson RJ. Clinician’s view of hypodontia. JADA 1980: 101: 283 – 286.

Pirinen S, Kentala A, Nieminen P, Varilo T, Thesleff I, Arte S. Recessively inherited lower incisor hypodontia J Med Genet 2001; 38: 551 – 556

Fekonja A. Hypodontia in orthodontically treated children. Eur J Orthod 2005; 27: 457 – 460.

Kirzioglu Z, Köseler Sentut T, Ozay Ertük MS, Karayilmaz H. Clinical features of hypodontia and associated dental anomalies: a retrospective study. Oral Diseases 2005; 11: 399 – 404.

Silva Meza R Radiographic assessment of congenitally missing teeth in orthodontic patients. Int J Paediatr Dent 2003; 13: 112 – 116.

Rasmussen P. Severe hypodontia: diversities in manifestations. J Clin Pediatr Dent 1999; 23: 179 – 188.

McKeown HF, Robinson DL, Elcock C, Al-Sharood M, Brook AH. Tooth dimensions in hypodontia patients, their unaffected relatives and a control group measured by a new image analysis system. Eur J Orthod 2002; 24: 131 – 141.

Miletich I, Sharpe PT. Normal and abnormal dental development. Hum Mol Genet 2003; 12: R69 – R73.

Kim JW, Simmer JP, Lin BPJ, Chu JC. Novel MSX2 frameshift causes autosomal dominant olygodontia. J Dent Res 2006; 85: 267 - 271.

Briceño I, Berrocal MC, González OA, Gutiérrez SJ, Ordoñez A, Torres D. Análisis clínico y molecular de la hipodoncia. Memorias IV - V Encuentro de Investigación en Ciencias Básicas en Odontología. URL disponible en: http://encolombia.com/odontologia/investigaciones/memorias-seminario.htm

Arboleda LA, Echeverri J, Restrepo LA, Marín ML, Vásquez G, Gómez JC, Manco HA, Pérez CM, Taborda E. Agenesia dental. Revisión bibliográfica y reporte de dos casos clínicos. Revista Facultad de Odontología Universidad de Antioquia 2006; 18: 47 – 54.

Bazán M. A congenitally missing canine in association with other dental disturbance: report of two cases. J Dent Child 1983; 50: 382 - 384.

Corrucini RS. An epidemiologic transition in dental occlusion in world populations. Am J Orthod 1984; 86: 419.

Correa MB, García-Robes M. Agenesia dentaria: Estudio familiar. Rev Cubana Ortod 1996; 11: 27 – 34.

How to Cite

Aránzazu Moya, G. C. (2018). HYPODONTIA: A FAMILIAL CASE REPORT. Ustasalud, 6(2), 131–134. https://doi.org/10.15332/us.v6i2.1810

Issue

Section

Case reports