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Original Research

Open Access

Orocraniofacial Findings and Dental Management of a Pediatric Patient with Dubowitz Syndrome

  • Garrocho-Rangel JA1,*,
  • Bueno-Rubio GA1
  • Martínez-Sandoval B1
  • Ruiz-Rodríguez MS1
  • Santos-Diaz MA1
  • Pozos-Guillén AJ1

1Pediatric Dentistry Posgraduate Program, Facultad de Estomatología, Universidad Autónoma de San Luis Potosí, México

DOI: 10.17796/jcpd.37.2.y5w316j142314073 Vol.37,Issue 2,December 2012 pp.203-206

Published: 01 December 2012

*Corresponding Author(s): Garrocho-Rangel JA E-mail: apozos@uaslp.mx

Abstract

Dubowitz syndrome is a rare genetic condition characterized by microcephaly, dysmorphic facial features and delayed general growth. It is transmitted through autosomal recessive inheritance. The purpose of this report is to describe the oral, craniofacial and systemic characteristics of a 7-year 11-month-old boy with Dubowitz syndrome and the dental management provided. The pediatric dentist should possess the ability to recognize this rare alteration, to provide dental treatment and to refer for the necessary medical and multidisciplinary treatment.

Keywords

Dubowitz syndrome, orocraniofacial findings, dental management

Cite and Share

Garrocho-Rangel JA,Bueno-Rubio GA,Martínez-Sandoval B,Ruiz-Rodríguez MS,Santos-Diaz MA,Pozos-Guillén AJ. Orocraniofacial Findings and Dental Management of a Pediatric Patient with Dubowitz Syndrome. Journal of Clinical Pediatric Dentistry. 2012. 37(2);203-206.

References

1. Dubowitz V. Familial low birth weight dwarfism with an unusual facies and a skin eruption. J Med Genet; 2: 12–17, 1965.

2. Tsukahara M, Opitz J. Dubowitz syndrome: review of 141 cases including 36 previously unreported patients. Am J Hum Genet; 63: 277–289, 1996.

3. Ballini A, Cantore S, Tullo D, Desiate A. Dental and craniofacial charac-teristics in a patient with Dubowitz syndrome: a case report. J Med Case Reports; 5: 38–42, 2011.

4. Gross R, Gorlin J, Opitz JM. The Dubowitz syndrome, further observa-tions. Z Kinderheilkd; 110: 175–187, 1971.

5. Chan KM, King NM. Dubowitz syndrome: report of a case with emphasis on the oral features. J Dent Child; 72: 100–103, 2005.

6. Wilhelm OL, Mehes K. Dubowitz syndrome. Acta Paediatr Hung; 27: 67–75, 1986.

7. Tsukahara M. Dubowitz syndrome. http://www.orpha.net/data/patho/GB/uk-dubowitz.pdf. 2001.

8. Jones KL. Recognizable patterns of human malformations (6th ed.). Phila-delphia: Saunders, pp. 100–101, 2006.

9. Wilroy RS, Tripton RE, Summit RL. The Dubowitz syndrome. Am J Med Genet; 2: 275–284, 1978.

10. Kuster W, Majewski F. The Dubowitz syndrome. Eur J Pediatr; 144: 574–578, 1986.

11. Goodman R, Gorlin RJ. Atlas of the face in genetic disorders (2nd ed.). St. Louis, MO: Mosby, pp. 266, 1977.

12. Nowicki MJ, Peterson RB. Dubowitz syndrome and achalasia: two rare conditions in a child. Clin Pediatr (Phila); 37: 197–200, 1998.

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