Dental anomalies are caused by complex interactions between genetic, epigenetic and
environmental factors during the long process of dental development. This process is …

Hypohidrotic (anhidrotic) ectodermal dysplasia (HED) is a congenital syndrome
characterized by sparse hair, oligodontia, and reduced sweating. It is caused by mutations in …

Tooth agenesis or hypodontia, failure to develop all normally developing teeth, is one of the
most common developmental anomalies in man. Common forms, including third molar …

Recent studies have detected mutations in the EDA gene, previously identified as causing X-
linked hypohidrotic ectodermal dysplasia (XLHED), in two families with X-linked non …

The history and the lessons learned from hypohidrotic ectodermal dysplasia (HED) may
serve as an example for the unraveling of the cause and pathogenesis of other ectodermal …

Genetics gains more and more importance in all areas of health care including craniofacial
surgery and dentistry. This does not mean that every patient will benefit from genetic …

Mutations in three functionally related genes EDA, EDAR and EDARDD have been reported
to cause hypohidrotic ectodermal dysplasia (HED), which is characterized by sparse hair …

OBJECTIVE: The purpose of this study was to clone and analyze mutation in the eda-A1
gene for hypohidrotic ectodermal dysplasia (HED), and to construct a new recombined …

Hypohidrotic ectodermal dysplasia (HED) is a rare skin disease characterized by
hypotrichosis, hypodontia and hypohidrosis. HED can be autosomal dominant, autosomal …

In the text, gene names are written in italics and protein names in CAPITALS following the
official recommendation of the nomenclature given by International Committee on …