Abstract
Ectodermal dysplasia (ED) is a rare hereditary disorder which is characterized by the defect of tissue of ectodermal origin. It is heterogeneous group of hereditary disorder which affects approximately one in every 100,000 births. Children who have ED may have various manifestations which may or may not involve teeth, skin, hair, nails, and sweat glands. Here, we present one such case of ectodermal dysplasia in 12-year-old patient.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Adesh University Journal of Medical Sciences & Research
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
