Ectodermal dysplasia: A case report

Ectodermal dysplasia (ED) is a rare group of inherited disorders with defects in the development one or more tissues derived from primary embryonic ectodermal derivatives. The inclusion ED does not include all derivatives and manifested defect skin, hair, teeth, eccrine glands. Dry frontal bossing, scanty eyebrows, hair follicles are common features seen these patients. patient may suffer high fever due to absence Intraoral findings partial complete teeth generalized spacing. It can be caused by genetic mutation, it also happen without family history. This case report presents 12-year-old female child hypohidrotic involving multidisciplinary approach that was beneficial both physiologically psychologically discussed this report.