A case report of ectodermal dysplasia with mandibular prognathism.
نویسندگان
چکیده
منابع مشابه
Report of a Case of Hypodontia due to Ectodermal Dysplasia: Early Rehabilitation with Overdenture
Alveolar ridge is underdeveloped in ectodermal dysplasia (ED). The available treatment plans include fixed, removable or implant-supported prostheses, alone or in combination. A 5 year-old boy was referred for treatment to the Department of Prosthodontics, Tehran University of Medical Sciences with the chief complaint of missing teeth. Prosthodontic treatment was performed to improve masticatio...
متن کاملEctodermal Dysplasia: A Case Report
Ectodermal dysplasia is a hereditary disease characterized by dysplasia of tissues of ectodermal origin. The incidence of ectodermal dysplasia is rare (1 in 100,000 birth). This case report discusses the features, classification and prosthetic treatment plan (upper partial denture and lower complete denture for upper partial and lower complete edentulous arches respectively). This treatment pla...
متن کاملHypohydrotic Ectodermal Dysplasia -a Case Report
Ectodermal dysplasia is a rare hereditary disorder. Its Hypohidrotic (HED) variant is also known as ChirstSiemens-Touraine syndrome. It is inherited as an Xlinked trait. Such Patients are characterized by the clinical manifestations of Hypodontia, Hypotrichosis, Hypohidrosis and a highly characteristic facial physiognomy. This article, reports a typical case of Hypohidrotic Ectodermal Dysplasia...
متن کاملHypohidrotic ectodermal dysplasia--a case report.
A case presented here is that of a nine year old male patient with total anodontia. Findings of this case as regards to the orofacial, radiographic and other general manifestations were suggestive of hypohidrotic ectodermal dysplasia. The dental problems were best managed by prosthetic replacement of dentition taking into consideration a design which would provide adequate relief for the preser...
متن کاملHereditary Ectodermal Dysplasia - A Case Report
Ectodermal dysplasia is an extremely rare genetic disorder characterized by faulty development of ectodermal structures. The tissues in which the primary defects occur are the skin, hair, nails, exocrine glands, and teeth. It usually affects the males and females are the carriers. The clinical features include sparse hair, abnormal or missing teeth, and inability to sweat due to lack of sweat g...
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ژورنال
عنوان ژورنال: Japanese Journal of Oral & Maxillofacial Surgery
سال: 1991
ISSN: 2186-1579,0021-5163
DOI: 10.5794/jjoms.37.387