Ectodermal dysplasia : a rare case report
Other Title(s)
تقرير لحالة نادرة من خلل التنسج الأديمي الظاهر
Author
Source
Journal of the Arab Board of Health Specializations
Issue
Vol. 23, Issue 1 (30 Jun. 2022), pp.50-52, 3 p.
Publisher
The Arab Board of Health Specializations
Publication Date
2022-06-30
Country of Publication
Syria
No. of Pages
3
Main Subjects
Abstract EN
The ectodermal dysplasias (EDs) comprise a large, heterogeneous group of inherited disorders that are defined by primary defects in the development of two or more tissues derived from embryonic ectoderm.
The primarily involved tissues are the skin and its appendages (hair follicles, eccrine glands, sebaceous glands, and nails) and teeth.
Although Thurnam published the first report of a patient with ED in 1848, the term ED was not coined until 1929 by Weech.
One such case report of ED is demonstrated here.
American Psychological Association (APA)
Sulayman, Umran. 2022. Ectodermal dysplasia : a rare case report. Journal of the Arab Board of Health Specializations،Vol. 23, no. 1, pp.50-52.
https://search.emarefa.net/detail/BIM-1431371
Modern Language Association (MLA)
Sulayman, Umran. Ectodermal dysplasia : a rare case report. Journal of the Arab Board of Health Specializations Vol. 23, no. 1 (2022), pp.50-52.
https://search.emarefa.net/detail/BIM-1431371
American Medical Association (AMA)
Sulayman, Umran. Ectodermal dysplasia : a rare case report. Journal of the Arab Board of Health Specializations. 2022. Vol. 23, no. 1, pp.50-52.
https://search.emarefa.net/detail/BIM-1431371
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 52
Record ID
BIM-1431371
