Ectodermal dysplasia (ED) is an inherited disorder that affects ectodermally derived organs, such as teeth. Pathogenesis is thought to involve an altered epithelium-mesenchymal interaction. ED patients have oligodontia (or sometimes anodontia) in addition to other abnormalities involving the skin, sweat glands, or hair. Many different subtypes have been introduced in the literature. This article describes the case of a 4-year-old patient who, after being diagnosed with ED, was put on a treatment plan that involved mandibular implants, reshaping of the maxillary primary central incisors, and prosthetic dental rehabilitation. Due to the child's rapid growth, both dentures were changed 9 months post-treatment. Two years posttreatment, the maxi...
Objectives: Ectodermal dysplasia (ED) is a relatively common sex-linked dermatitis characterized by ...
Alveolar ridge is underdeveloped in ectodermal dysplasia (ED). The available treatment plans include...
Ectodermal dysplasia is the term used to describe a large and heterogenic group of congenital disord...
Congenital absence of multiple teeth and poorly developed alveolar ridges are associated with ecto-d...
Background and Aim: Ectodermal dysplasia (ED) is a hereditary disease that affects ectodermal tissue...
Ectodermal dysplasia (ED) is a genetically heterogeneous condition resulting from clinical anomalies...
Ectodermal dysplasia (ED) is a rare congenital disease that affects several ectodermal structures. C...
Ectodermal dysplasia (ED) is a genetically heterogeneous condition resulting from clinical anomalies...
Introduction Ectodermal dysplasia syndromes are a heterogeneous group of inherited diseases charact...
The purpose of this article is to report the clinical course and 6-year follow-up of a child with ec...
Abstract Ectodermal dysplasia (ED) is a congenital syndrome characterized by developmental failure ...
Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction...
Ectodermal dysplasia (ED) is a genetic disorder that is often associated with anomalies of teeth suc...
Introduction: Ectodermal dysplasia (ED) is an inherited disruption of two or more tissues and struct...
Ectodermal Dysplasia (ED) is an inherent disorder which affects ectodermal tissues, including teeth....
Objectives: Ectodermal dysplasia (ED) is a relatively common sex-linked dermatitis characterized by ...
Alveolar ridge is underdeveloped in ectodermal dysplasia (ED). The available treatment plans include...
Ectodermal dysplasia is the term used to describe a large and heterogenic group of congenital disord...
Congenital absence of multiple teeth and poorly developed alveolar ridges are associated with ecto-d...
Background and Aim: Ectodermal dysplasia (ED) is a hereditary disease that affects ectodermal tissue...
Ectodermal dysplasia (ED) is a genetically heterogeneous condition resulting from clinical anomalies...
Ectodermal dysplasia (ED) is a rare congenital disease that affects several ectodermal structures. C...
Ectodermal dysplasia (ED) is a genetically heterogeneous condition resulting from clinical anomalies...
Introduction Ectodermal dysplasia syndromes are a heterogeneous group of inherited diseases charact...
The purpose of this article is to report the clinical course and 6-year follow-up of a child with ec...
Abstract Ectodermal dysplasia (ED) is a congenital syndrome characterized by developmental failure ...
Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction...
Ectodermal dysplasia (ED) is a genetic disorder that is often associated with anomalies of teeth suc...
Introduction: Ectodermal dysplasia (ED) is an inherited disruption of two or more tissues and struct...
Ectodermal Dysplasia (ED) is an inherent disorder which affects ectodermal tissues, including teeth....
Objectives: Ectodermal dysplasia (ED) is a relatively common sex-linked dermatitis characterized by ...
Alveolar ridge is underdeveloped in ectodermal dysplasia (ED). The available treatment plans include...
Ectodermal dysplasia is the term used to describe a large and heterogenic group of congenital disord...