A high number of patients have one or more missing tooth and it is estimated that one in four
American subjects over the age of 74 have lost all their natural teeth. Many options exist to …

Ectodysplasin A related hypohidrotic ectodermal dysplasia (XLHED) is a well-studied fetal
developmental disorder in mammals that mainly affects ectodermal structures. It has been …

Hypohidrotic ectodermal dysplasia (HED) is a rare congenital disorder that associates with
dental manifestations of anodontia, hypodontia, and atrophic alveolar ridges. Although the …

Ectodermal dysplasias (ED) are a group of rare genetic disorders characterized by
congenital defects involving two or more ectodermal structures. Christ-Siemens-Touraine …

Abstract Christ–Siemens–Touraine syndrome/hypohidrotic ectodermal dysplasia (HED) is a
heterogeneous group of inherited disorders with primary defects in tissues derived from …

Ectodermal dysplasias are a rare group of heritable disorders involving the ectodermal
derivatives with only a few published reports involving its anaesthetic management. We …

Ectodermal dysplasia is a rare disorder. Christ-Siemens-Touraine syndrome (Hypohidrotic
Ectodermal dysplasia (HED)) is a diffuse, non-progressive disease present at birth and …

La displasia ectodérmica (DE) es un trastorno genético que se caracteriza por alteraciones
que afectan las estructuras derivadas del ectodermo; usualmente el síndrome presenta …

Hypohidrotic ectodermal dysplasia (HED) is a rare hereditary disorder that affects tissues
derived from the ectoderm including hair, teeth and sweat glands. EDA is the major …

Ectodermal dysplasia (ED) is a hereditary disease characterized by anomalies in the
structures of ectodermal origin. This report aims to determine the oral features of patients …