Oral Manifestations of schimmelpenning syndrome: case report and review of literature

A. Murakami, F. Skovby, J. O. Andreasen, M. M. Cohen, B. L. Jensen, S. Kreiborg

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

Schimmclpenning syndrome (SS) is characterised by specific skin manifestations, skeletal defects, and central nervous system abnormalities. Here, the SS is briefly reviewed, and the oral and dental manifestations arc described in a patient whose medicalflndings were previously published and included severe hypophosphatemic rickets. Significant oral and dental features includedpapillomatous lesions of thegingiva, hemihyperplasia (hemihypertrophy) of the tongue, bone cysts, aplasia of teeth, enlarged pulp chambers, hypoplastic or absent enamel, and an odontodvsolasia-like permanent tooth.

Original languageEnglish
Pages (from-to)744-748
Number of pages5
JournalAnnals of the Academy of Medicine, Singapore
Volume28
Issue number5
Publication statusPublished - 1999
Externally publishedYes

ASJC Scopus Subject Areas

  • General Medicine

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