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Sotos syndrome with enamel hypoplasia: a case report

  • Mikiko Inokuchi1,*,
  • Jouji Nomura1
  • Yoshihiko Mtsumura1
  • Motoko Sekida1
  • Toshiro Tagawa1

1Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Mie University, Japan

DOI: 10.17796/jcpd.25.4.n52851t26173843u Vol.25,Issue 4,October 2001 pp.313-316

Published: 01 October 2001

*Corresponding Author(s): Mikiko Inokuchi E-mail: XXX

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Abstract

A rare case of Sotos syndrome with enamel hypoplasia is described. Dental abnormalities include

enamel hypoplasia, expansion of the pulp cavity, high arched palate, and absence of the bilateral premolar

teeth of the mandible.


Cite and Share

Mikiko Inokuchi,Jouji Nomura,Yoshihiko Mtsumura,Motoko Sekida,Toshiro Tagawa. Sotos syndrome with enamel hypoplasia: a case report. Journal of Clinical Pediatric Dentistry. 2001. 25(4);313-316.

URL:

https://www.jocpd.com/articles/10.17796/jcpd.25.4.n52851t26173843u

References

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11. Suzuki N, Kyo K. Sotos syndrome associated with West syndrome and a visual disorder. Pediatrics International 41: 395-398, 1999.

12. Butler MG, Dijkstra PF. Metacarpophalangeal pattern profile analysis in Sotos syndrome: A follow-up report on 34 subjects. Am J Med Genetics 29: 143-147, 1988.

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15. Shields ED, Bixler D, El-Kafrawy AM. A proposed classification for heritable human dentine defects with a description of a new entity. Archs oral Biol 18: 543-553, 1973.

16. Waldron CA. Autosomal recessive pigmented hypomaturation ameleogenesis imperfecta. Oral Surgery 36: 367-382, 1973.


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