Ectodermal dysplasia (ED) is a genetic disorder that is often associated with anomalies of teeth such as hypodontia and oligodontia. Individuals affected by ED have abnormalities of the epithelial tissue of the hair, nails, teeth, or sweat glands. Implant-prosthetic rehabilitation is often necessary because the severity of disease may limit other treatment options. This is a report of a 30-year-old man affected by ED who exhibited severe hypodontia and atrophy of the jaws. Radiographic and clinical evaluations showed inadequate quantity of bone for immediate implant rehabilitation. Osteogenetic vertical distraction and grafting of autogenous bone were performed to obtain the correct bone volume, and implants were inserted in the anterior ma...
Full mouth rehabilitation in patients with ectodermal dysplasia (ED) is difficult to manage, especia...
Type-I ectodermal dysplasia (Christ-Siemens-Touraine syndrome) is characterized by clinical triad of...
Ectodermal Dysplasia is a hereditary disease characterized by a congenital dysplasia of one or more ...
Ectodermal dysplasia (ED) is an inherited disorder characterized by abnormality of ectodermally deri...
Ectodermal dysplasia (ED) comprises a large, heterogeneous group of inherited disorders that are def...
Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction...
AbstractEctodermal dysplasia (ED) comprises a large heterogeneous group of inherited disorders that ...
Ectodermal dysplasia (ED) is a congenital syndrome characterized chiefly by abnormalities of tissues...
Ectodermal dysplasia is a rare group of disorders affecting the hair, nails, teeth and sweat glands ...
Ectodermal dysplasia (ED) is an inherited disorder that affects ectodermally derived organs, such as...
Ectodermal dysplasia (ED) is a congenital syndrome characterized chiefly by abnormalities of tissues...
Ectodermal dysplasia is a rare hereditary disorder associated with dysplasia of the tissues of ectod...
Congenital absence of multiple teeth and poorly developed alveolar ridges are associated with ecto-d...
Ectodermal dysplasia is a genetic disease caused by incorrect development of the epidermis and cuta...
Ectodermal dysplasia is the term used to describe a large and heterogenic group of congenital disord...
Full mouth rehabilitation in patients with ectodermal dysplasia (ED) is difficult to manage, especia...
Type-I ectodermal dysplasia (Christ-Siemens-Touraine syndrome) is characterized by clinical triad of...
Ectodermal Dysplasia is a hereditary disease characterized by a congenital dysplasia of one or more ...
Ectodermal dysplasia (ED) is an inherited disorder characterized by abnormality of ectodermally deri...
Ectodermal dysplasia (ED) comprises a large, heterogeneous group of inherited disorders that are def...
Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction...
AbstractEctodermal dysplasia (ED) comprises a large heterogeneous group of inherited disorders that ...
Ectodermal dysplasia (ED) is a congenital syndrome characterized chiefly by abnormalities of tissues...
Ectodermal dysplasia is a rare group of disorders affecting the hair, nails, teeth and sweat glands ...
Ectodermal dysplasia (ED) is an inherited disorder that affects ectodermally derived organs, such as...
Ectodermal dysplasia (ED) is a congenital syndrome characterized chiefly by abnormalities of tissues...
Ectodermal dysplasia is a rare hereditary disorder associated with dysplasia of the tissues of ectod...
Congenital absence of multiple teeth and poorly developed alveolar ridges are associated with ecto-d...
Ectodermal dysplasia is a genetic disease caused by incorrect development of the epidermis and cuta...
Ectodermal dysplasia is the term used to describe a large and heterogenic group of congenital disord...
Full mouth rehabilitation in patients with ectodermal dysplasia (ED) is difficult to manage, especia...
Type-I ectodermal dysplasia (Christ-Siemens-Touraine syndrome) is characterized by clinical triad of...
Ectodermal Dysplasia is a hereditary disease characterized by a congenital dysplasia of one or more ...