1/61. The use of tricalcium phosphate to preserve alveolar bone in a patient with ectodermal dysplasia: a case report.The prosthodontic management of the child with ectodermal dysplasia is made difficult because of the under-development of the alveolar ridges. This paper describes a case where tricalcium phosphate was placed in sockets immediately following the extraction of the primary incisor teeth to help maintain alveolar bone width, offering a valuable alternative treatment option in the prosthodontic management of the child patient with ectodermal dysplasia.- - - - - - - - - - ranking = 1keywords = alveolar ridge, alveolar, ridge (Clic here for more details about this article) |
2/61. Localized soft tissue ridge augmentation at phase 2 implant surgery: a case report.A case of congenitally missing maxillary lateral incisors is presented to illustrate a modification of Abrams's roll technique. Buccal releasing incisions are avoided by using an intrasulcular incision on the adjacent teeth. The tissue overlying the cover screw is transferred between the buccal cortical bone and the buccal masticatory mucosa, thus correcting the localized buccal ridge atrophy.- - - - - - - - - - ranking = 0.13423900045001keywords = ridge (Clic here for more details about this article) |
3/61. Restoration of congenitally missing lateral incisors: a case report.parents and dentists are forced to make a decision early in a young patient's life when it is learned that the lateral incisors are missing. For many years the treatment has been to either move the cuspids into the lateral incisor sites or retain the teeth in their natural environment and restore the defect with a bonded or fixed bridge. With the advent of new designs in dental implants and their abutments, it is possible to consider replacing missing single teeth with implant-borne prostheses. Often-times, because of the limited residual bone and proximity of adjacent roots, placing conventional cylinder or screw-type implants is difficult. This article demonstrates the advantages of using a tapered-step implant, immediate one-stage surgery, and temporization in replacing congenitally missing laterals.- - - - - - - - - - ranking = 0.026847800090002keywords = ridge (Clic here for more details about this article) |
4/61. Witkop tooth and nail syndrome: report of two cases in a family.tooth and nail syndrome, an autosomal dominant condition, is characterized by hypodontia and nail dysplasia. Mandibular incisors, second molars and maxillary canines are the most frequently missing teeth. tooth shape may vary and conical and narrow crowns are common. Nail dysplasia affects fingernails and toenails and is often more severe in childhood. nails may be spoon-shaped, ridged, slow growing and easily broken. The clinical and radiographic features of a father and son presenting with this rare condition are described.- - - - - - - - - - ranking = 0.026847800090002keywords = ridge (Clic here for more details about this article) |
5/61. Hypohidrotic 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 preservation of the ridges which were thin and underdeveloped to the absence of teeth.- - - - - - - - - - ranking = 0.026847800090002keywords = ridge (Clic here for more details about this article) |
6/61. Restorative dentistry using a multidisciplinary approach.Multidisciplinary treatment was essential for this patient to optimally manage the occlusion and missing teeth. When the space distribution was completed, ridge management procedures for pontic site development were accomplished. The final restorative treatment required was actually minimized to a 7-unit fixed partial denture. It was apparent the multidisciplinary treatment was essential to predictably manage this patient by decreasing risk and ensuring a long-term strategy for enhanced patient satisfaction.- - - - - - - - - - ranking = 0.026847800090002keywords = ridge (Clic here for more details about this article) |
7/61. dyskeratosis congenita: report of a case.dyskeratosis congenita is a rare multisystem condition involving mainly the ectoderm. It is characterized by a triad of reticular skin pigmentation, nail dystrophy and leukoplakia of mucous membranes. Oral and dental abnormalities may also be present. Complications are a predisposition to malignancy and bone marrow involvement with pancytopenia. The case of a 14-year-old girl is described who presented with several of the characteristic systemic features of this condition, together with the following oral features: hypodontia, diminutive maxillary lateral incisors, delayed dental eruption, crowding in the maxillary premolar region, short roots, poor oral hygiene, gingival inflammation and bleeding, alveolar bone loss, caries and a smooth atrophic tongue with leukoplakia. Although this condition is rare, dental surgeons should be aware of the dental abnormalities that exist and the risk of malignant transformation within the areas of leukoplakia.- - - - - - - - - - ranking = 0.030021320188134keywords = alveolar (Clic here for more details about this article) |
8/61. Clinical features of incontinentia pigmenti with emphasis on dermatoglyphic findings.incontinentia pigmenti is a syndrome characterized by both systemic and oral manifestations. Presented here are the dental, clinical, radiological, genetic and dermatoglyphic findings of a 6 year old female case and her family members. The following features were apparent: oligodontia in maxillary and mandibular arches in both dentition, peg-shaped incisors and brown lesions on the body surface. No other problems were observed. The case had remarkable dermatoglyphic findings such as hypothenar loops associated with distally displaced axial triradii on both palms, reduced total finger and summed palmar a-b ridge-counts, decreasing plantar pattern intensity on the left sole. The other family members had similar dermatoglyphic characteristics. The paternal grand father, the father and the brother had eye defects.- - - - - - - - - - ranking = 0.026847800090002keywords = ridge (Clic here for more details about this article) |
9/61. A newly recognized syndrome of skeletal dysplasia with opalescent and rootless teeth.A Thai girl with skeletal dysplasia and dental anomalies was seen. Her anomalies consisted of disproportionately short stature, short neck, broad and depressed nasal bridge, broad chest in the anteroposterior dimension, kyphosis, widely spaced nipples, and protruded abdomen. Radiographic testing indicated that she had a large sella turcica, platyspondyly, hypoplastic acetabulum, and a small body of mandible. Both her deciduous and permanent teeth were equally opalescent, and most were rootless, with root development of the mandibular teeth more severely affected. Some maxillary roots were extremely short and tapered. Hypodontia was also observed. These findings represent a unique and hitherto undescribed syndrome of skeletal dysplasia with concomitant dental anomalies.- - - - - - - - - - ranking = 0.026847800090002keywords = ridge (Clic here for more details about this article) |
10/61. Overlay removable partial dentures for a patient with ectodermal dysplasia: a clinical report.The orofacial characteristics of ectodermal dysplasia include anodontia or hypodontia, hypoplastic conical teeth, underdevelopment of the alveolar ridges, frontal bossing, a depressed nasal bridge, protuberant lips, and hypotrichosis. patients with this disease often need complex prosthetic treatment. The options for a definitive treatment plan may include fixed, removable, or implant-supported prostheses, singly or in combination. However, financial constraints and other priorities can prevent patients from choosing the most desirable treatment. This clinical report describes the diagnosis and treatment of ectodermal dysplasia in an 18-year-old man. The treatment included interim removable partial dentures fabricated to establish an acceptable therapeutic occlusal vertical dimension, followed by definitive overlay removable partial dentures and composite restorations.- - - - - - - - - - ranking = 0.87674119914933keywords = alveolar ridge, alveolar, ridge (Clic here for more details about this article) |
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