Ectodermal dysplasia has several characteristic signs and symptoms, including anadontia or hypodontia, conical and hypoplastic teeth, atrophic alveolar ridges, protuberant lips, and hypotrichosis. Definitive treatment options for these patients are several including fixed, removable or implant-supported prostheses. Economic limitations or other priorities can prevent patients from choosing the most desirable treatment. This clinical report describes the prosthetic rehabilitation of a patient with ectodermal dysplasia. The treatment developed an overlay immediate removable partial denture fabricated to reconstruct acceptable occlusal vertical dimension, function and esthetics. A 2-year period of follow up showed the minor chipping of composi...
Ectodermal dysplasia (ED) represents a disorder group characterised by abnormal development of the e...
Objective: To illustrate the problems of partial anodontia and replacement of missing teeth and bone...
Ectodermal dysplasias are rare hereditary disorders characterized by abnormal development of certain...
The orofacial characteristics of ectodermal dysplasia include anodontia or hypodontia, hypoplastic c...
Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction...
Ectodermal dysplasia is a rare hereditary disorder associated with dysplasia of the tissues of ectod...
Type-I ectodermal dysplasia (Christ-Siemens-Touraine syndrome) is characterized by clinical triad of...
Alveolar ridge is underdeveloped in ectodermal dysplasia (ED). The available treatment plans include...
Introduction Ectodermal dysplasia syndromes are a heterogeneous group of inherited diseases charact...
Introduction: Ectodermal dysplasia (ED) is a hereditary disorder characterized by developmental dist...
The management of the patients with ectodermal dysplasia has always been a challenge for clinicians ...
Ectodermal dysplasia represents a group of inherited conditions in which two or more ectodermally de...
Full mouth rehabilitation in patients with ectodermal dysplasia (ED) is difficult to manage, especia...
Oral clinical manifestations of ectodermal dysplasia are in a wide variety, ranging from the presenc...
Abstract Ectodermal dysplasia (ED) is a congenital syndrome characterized by developmental failure ...
Ectodermal dysplasia (ED) represents a disorder group characterised by abnormal development of the e...
Objective: To illustrate the problems of partial anodontia and replacement of missing teeth and bone...
Ectodermal dysplasias are rare hereditary disorders characterized by abnormal development of certain...
The orofacial characteristics of ectodermal dysplasia include anodontia or hypodontia, hypoplastic c...
Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction...
Ectodermal dysplasia is a rare hereditary disorder associated with dysplasia of the tissues of ectod...
Type-I ectodermal dysplasia (Christ-Siemens-Touraine syndrome) is characterized by clinical triad of...
Alveolar ridge is underdeveloped in ectodermal dysplasia (ED). The available treatment plans include...
Introduction Ectodermal dysplasia syndromes are a heterogeneous group of inherited diseases charact...
Introduction: Ectodermal dysplasia (ED) is a hereditary disorder characterized by developmental dist...
The management of the patients with ectodermal dysplasia has always been a challenge for clinicians ...
Ectodermal dysplasia represents a group of inherited conditions in which two or more ectodermally de...
Full mouth rehabilitation in patients with ectodermal dysplasia (ED) is difficult to manage, especia...
Oral clinical manifestations of ectodermal dysplasia are in a wide variety, ranging from the presenc...
Abstract Ectodermal dysplasia (ED) is a congenital syndrome characterized by developmental failure ...
Ectodermal dysplasia (ED) represents a disorder group characterised by abnormal development of the e...
Objective: To illustrate the problems of partial anodontia and replacement of missing teeth and bone...
Ectodermal dysplasias are rare hereditary disorders characterized by abnormal development of certain...