Close Menu

Books in a Library

A Rare Case: Epidermolysis Bullosa in a Child Patient with Amelogenesis Imperfecta

DOI: 
10.7727/wimj.2015.339

ABSTRACT

Epidermolysis bullosa (EB) is an inherited disorder affecting the skin and mucous membranes, characterized by blister formation following minor trauma. It is a chronic mechanobullous disease related to the specific abnormal or absent proteins. The disease is associated with conspicuous clinical and oral manifestations. The oral involvement of EB includes generalized enamel hypoplasia, dental caries, limited mouth opening, ankyloglossia, microstomia and obliteration of the vestibule.

Amelogenesis imperfecta (AI) is a hereditary disorder with dental enamel defects and enamel hypoplasia both in deciduous and permanent dentition.

There is very limited information in the literature, which indicate the presence of EB together with AI.

The aim of this report is to present the clinical and radiographic manifestations and dental management of EB simplex in a child patient with hypoplastic form of AI. 

Accepted: 
25 Aug, 2015
PDF Attachment: 
e-Published: 26 Feb, 2016

Disclaimer

Manuscripts that are “Published at Acceptance” have been peer reviewed and accepted for publication by the Editorial Board of the West Indian Medical Journal. They may appear prior to being copy edited or formatted in the style guide of this Journal. The contents of the manuscript may change before it is published in its final form. While accepted manuscripts are not yet assigned a volume, issue, or page numbers, they can be cited using the DOI and date of e-publication. See our Instructions for Authors on how to properly cite manuscripts at this stage. Manuscripts in this section will be removed once they have been assigned to a volume and issue, but will still retain the DOI and date of e-publication.

Top of Page