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Published in: Journal of Medical Case Reports 1/2009

Open Access 01-12-2009 | Case report

Incontinentia pigmenti presenting as hypodontia in a 3-year-old girl: a case report

Authors: Dárcio Kitakawa, Patrícia Campos Fontes, Fernando Augusto Cintra Magalhães, Janete Dias Almeida, Luiz Antonio Guimarães Cabral

Published in: Journal of Medical Case Reports | Issue 1/2009

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Abstract

Introduction

Incontinentia pigmenti or Bloch-Sulzberger syndrome is a rare X-linked dominant disease that mainly affects the skin, eyes, hair, central nervous system and teeth. The disease is predominant among women. Although dermatologic manifestations are among the most important aspects for the diagnosis of the syndrome, they are less damaging to the patient and do not require treatment. However, oral involvement characterized by hypodontia of deciduous and permanent teeth is important for the diagnosis and treatment of the patient.

Case presentation

We report the case of a 3-year-old girl with ophthalmologic and neurologic disturbances, cutaneous manifestations and hypodontia. Since the patient did not present more damaging manifestations such as neurologic and/or ophthalmologic problems, her most severe complications were related to dental anomalies. The importance of integrated dental treatment, which combines pediatric dentistry, orthodontics and conventional prosthesis, is emphasized.

Conclusion

Hypodontia is a frequent finding in incontinentia pigmenti, and dentists should be aware of this condition in order to help with the diagnosis.
Appendix
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Metadata
Title
Incontinentia pigmenti presenting as hypodontia in a 3-year-old girl: a case report
Authors
Dárcio Kitakawa
Patrícia Campos Fontes
Fernando Augusto Cintra Magalhães
Janete Dias Almeida
Luiz Antonio Guimarães Cabral
Publication date
01-12-2009
Publisher
BioMed Central
Published in
Journal of Medical Case Reports / Issue 1/2009
Electronic ISSN: 1752-1947
DOI
https://doi.org/10.1186/1752-1947-3-116

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