Significados de ectodermal dysplasia en inglés

Four men and 1 woman with ectodermal dysplasia syndrome were treated.

Hypohidrotic ectodermal dysplasia should be included in the differential diagnosis of fever of unknown origin.

In this study, plastic rehabilitation was developed to correct the special features of patients with ectodermal dysplasia.

Hay-Wells syndrome is a rare form of ectodermal dysplasia initially described by Hay and Wells in 1976.

Moreover, p63-null mice displayed abnormal epithelial development and germ-line human mutations were found to cause ectodermal dysplasia.

Mutations in genes encoding components of the EDA pathway disrupt normal appendage development, leading to the human disorder hypohidrotic ectodermal dysplasia.

The term ectodermal dysplasias includes many disorders that share some clinical features such as involvement of one or several ectodermal structures and congenital origin.