National Foundation for Ectodermal Dysplasia’s “Parameters of Oral Health Care for Individuals Affected by Ectodermal Dysplasia Syndromes.”2 Refer to that document for care of children with ectodermal dysplasia
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چکیده
Purpose The American Academy of Pediatric Dentistry (AAPD) recognizes that pediatric dentists are uniquely qualified to manage the oral health care needs of children with heritable dental developmental anomalies. These children have multiple, complex problems as their dental conditions affect both form and function and can have significant psychological impact. These conditions may present early in life and require both immediate intervention and management of a protracted nature, including coordination of multi-disciplinary care. The AAPD’s Guideline on Management of Dental Patients with Special Health Care Needs1 alludes to this patient population but does not make specific treatment recommendations for the oral manifestations of such diagnoses. This guideline is intended to address the diagnosis, principles of management, and objectives of therapy of children with heritable dental developmental anomalies rather than provide specific treatment recommendations. This guideline will focus on the following heritable dental developmental anomalies: amelogenesis imperfecta (AI), dentinogenesis imperfecta (DI), and dentin dysplasia (DD). Ectodermal dysplasia has been thoroughly studied and reported in the National Foundation for Ectodermal Dysplasia’s “Parameters of Oral Health Care for Individuals Affected by Ectodermal Dysplasia Syndromes.”2 Refer to that document for care of children with ectodermal dysplasia.
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National Foundation for Ectodermal Dysplasia’s “Parameters of Oral Health Care for Individuals Affected by Ectodermal Dysplasia Syndromes.” Refer to that document for care of children with ectodermal dysplasia
Purpose The American Academy of Pediatric Dentistry (AAPD) recognizes that pediatric dentists are uniquely qualified to manage the oral health care needs of children with heritable dental developmental anomalies. These children have multiple, complex problems as their dental conditions affect both form and function and can have significant psychological impact. These conditions may present earl...
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Background and Aim: Ectodermal dysplasia (ED) is a hereditary disease that affects ectodermal tissues. Its oral manifestations include hypodontia or oligodontia, which cause the reduction of the height and width of the alveolar ridge. Considering numerous difficulties that these patients encounter with regard to facial appearance, talking, and chewing, their rehabilitation has a major influence...
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Objectives: Ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) is a rare syndrome with features of ectrodactyly, ectodermal dysplasia and cleft lip/palate. This study presents an Iranian case with classic features and oral complications. Case: We report a 20-year old female with all manifestations of this syndrome. The simultaneous presence of these three malformations is extremely r...
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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...
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Objectives: Ectodermal dysplasia (ED) is a relatively common sex-linked dermatitis characterized by congenital dysplasia of one or more ectodermal structures and their accessory appendages. Common manifestations include fragile skin and nails, defective teeth and salivary glands, frontal bossing with prominent supra orbital ridges, nasal bridge depression and protuberant lips. Teeth are often f...
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