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Original Research

Open Access

Rapp-Hodgkin Syndrome: Clinical and Dental Findings

  • Gul Tosun1,*,
  • Ulku Elbay1

1Department of Pediatric Dentistry, Faculty of Dentistry. Selçuk University Konya /Turkey

DOI: 10.17796/jcpd.34.1.kr015833p1qg6873 Vol.34,Issue 1,January 2010 pp.71-76

Published: 01 January 2010

*Corresponding Author(s): Gul Tosun E-mail: gultosun@hotmail.com

Abstract

Rapp-Hodgkin syndrome is a rare form of ectodermal dysplasia involving the hair, eyes, sweat glands, nails,teeth and palate. This syndrome is characterized by stiff, sparse hair with the appearance of steel wool,sparse eyebrows and lashes, cleft palate, absence of lacrimal punctae, epiphora, a decreased number of sweat glands, and dystrophic nails. Cleft palate, hypodontia, abnormal tooth shape, multiple caries, delayed eruption of teeth are the main oral manifestations. In this paper we describe the clinical and dental findings of this syndrome in a 7 year old girl referred to the dental clinic because of severe tooth ache. The dental treatment included root canal treatment, composite restorations, extractions and removable prostheses. This paper highlights features of Rapp-Hodgkin Syndrome and its dental rehabilitation.

Keywords

Rapp-Hodgkin syndrome, hypodontia, cleft palate

Cite and Share

Gul Tosun,Ulku Elbay. Rapp-Hodgkin Syndrome: Clinical and Dental Findings. Journal of Clinical Pediatric Dentistry. 2010. 34(1);71-76.

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