Ectodermal dysplasia - A rare case report.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 31681695.
- Also identified by DOI 10.4103/jfmpc.jfmpc_625_19 and PMC identifier 6820434.
- Licence recorded as CC BY-NC-SA.
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Abstract
Ectodermal dysplasia (ED) is a rare genetic disease caused by developmental disturbances of embryonic ectoderm derived tissues, organs, and other accessory appendages. The congenital missing of teeth is usually bilateral. Anodontia or hypodontia may be associated with other ectodermal disturbances, such as anhidrosis, asteatosis, hypotrichosis, and salivary glands defects. One such case report of ED is demonstrated here.