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Zimmermann-Laband Syndrome: A Case Report

  • Sawaki K1
  • Mishima K1,*,
  • Sato A1
  • Goda Y1
  • Osugi A1
  • Nakano M1

1Department of Oral and Maxillofacial Surgery, Graduate School of Medicine, Yamaguchi University. Minamikogushi 1-1-1, Ube City, Yamaguchi, 755-8505, Japan.

DOI: 10.17796/jcpd.36.3.k854128176u764l8 Vol.36,Issue 3,May 2012 pp.297-300

Published: 01 May 2012

*Corresponding Author(s): Mishima K E-mail: kmishima@yamaguchi-u.ac.jp

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Abstract

Zimmermann-Laband syndrome is a very rare disorder characterized by gingival fibromatosis, abnormalities of soft cartilages of the nose and/or ears, hypoplastic or absent nails and terminal phalanges, joint hypermobility, hypatoslenomegaly, mild hirsutism and learning difficulties. Early presentation of Zimmermann-Laband syndrome in a newborn has rarely been described. This paper describes a newborn patient with Zimmermann-Laband syndrome.

Keywords

gingival fibromatosis, gingival enlargement, Zimmermann-Laband syndrome, children.

Cite and Share

Sawaki K,Mishima K,Sato A,Goda Y,Osugi A,Nakano M. Zimmermann-Laband Syndrome: A Case Report. Journal of Clinical Pediatric Dentistry. 2012. 36(3);297-300.

URL:

https://www.jocpd.com/articles/10.17796/jcpd.36.3.k854128176u764l8

References

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