Esthetic Rehabilitation of Familial Hypodontia: A Case Report
نویسندگان
چکیده
منابع مشابه
Esthetic Rehabilitation: A Case Report
One of the major focus of current restorative and prosthodontic dental treatment is on restoration of esthetics. For a treatment procedure to be successful, good communication with the patient to understand his/her functional and esthetic expectation is essential. During treatment planning phase, use of a diagnostic anatomic wax up helps the dentist to effectively communicate the final esthetic...
متن کاملFamilial Hypodontia: A Case Series.
The phenomenon of congenitally missing teeth has been described with different names: hypodontia, oligodontia, anodontia, congenitally missing teeth and dental agenesis. The present paper reports familial hypodontia, involving two siblings from a single family. Case I reported the absence of 18, 12, 22 and 31 teeth whereas case II reported the absence of 31 and 41. On the evaluation of the two ...
متن کاملReport 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 کاملFunctional and esthetic rehabilitation for a preschooler child using modified Groper's appliance: a clinical case report
Introduction: Premature loss of primary teeth affects child's nutrition, sleep, growth, and self-confidence. Besides, it can cause undesirable movement of the primary or permanent teeth. Case presentation: This paper reports a 5.5-year old boy presenting with severe-early childhood caries, who had suffered from early extraction of some primary teeth as well as several other dental problems. Af...
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Abstract Familial hypercholesterolemia (FH) is a hereditary dislipidemia. Patients present with extremely high level of low-density lipoprotein cholesterol (LDL-C), which is due to mutation in the gene of LDL receptor. Homozygous patients (HoFH) whose incidence is 1 in 1.000.000 are at high risk of premature aortic valve stenosis, and coronary artery atherosclerosis. In homozygous individual...
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ژورنال
عنوان ژورنال: Birat Journal of Health Sciences
سال: 2017
ISSN: 2542-2804,2542-2758
DOI: 10.3126/bjhs.v1i1.17104