Ectodermal dysplasia - A rare case report
Poulomi Bhakta, Bhavna Barthunia, Haritma Nigam and 1 more
Journal of Family Medicine and Primary Care · 2019
doi:10.4103/jfmpc.jfmpc_625_19 (opens in a new tab)
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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.
Abstract licence: CC BY-NC-SA
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