Management of dentin dysplasia and facial disharmony
dc.contributor.author | Chamberlain, Barbara B. | en_US |
dc.contributor.author | Hayward, James R. (James Rogers) | en_US |
dc.date.accessioned | 2010-06-01T18:34:21Z | |
dc.date.available | 2010-06-01T18:34:21Z | |
dc.date.issued | 1983-05 | en_US |
dc.identifier.citation | Chamberlain, Barbara B.; Hayward, J. R. (1983). "Management of dentin dysplasia and facial disharmony." Special Care in Dentistry 3(3): 113-116. <http://hdl.handle.net/2027.42/71777> | en_US |
dc.identifier.issn | 0275-1879 | en_US |
dc.identifier.issn | 1754-4505 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/71777 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6574606&dopt=citation | en_US |
dc.description.abstract | Patients with unusual congenital dental anomalies are often referred to the hospital dentistry team for evaluation and treatment recommendations. Communication between oral surgeon, orthodontist, pedodontist, periodontist, and prosthodontist after a combined single examination may simplify the treatment alternatives and save the patient the frustration and confusion of seeking treatment from a number of specialists. When necessary, com- bined treatment can be efficiently coordinated at the original consultation appointment. The recommendations of each specialist are then recorded together in the hospital record. This' simplifies follow-up treatment and allows for easy transfer of information should the patient move to another location. In complex treat- ment cases, the pooling of dental specialist re- sources may permit conservatism and answer the patient's needs with lifetime perspectives. | en_US |
dc.format.extent | 1566424 bytes | |
dc.format.extent | 3109 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.publisher | Blackwell Publishing Ltd | en_US |
dc.rights | 1983 Special Care Dentistry Association and Blackwell Publishing | en_US |
dc.title | Management of dentin dysplasia and facial disharmony | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Dentistry | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | maxillofacial prosthodontist at the University of Michigan Hospitals and assistant professor at the University of Michigan School of Dentistry, Ann Arbor, 48109 | en_US |
dc.contributor.affiliationum | Oral surgeon recently retired from his practice at the University of Michigan Hospitals and as chairman, department of oral and maxillofacial surgery, University of Michigan School of Dentistry, Ann Arbor | en_US |
dc.identifier.pmid | 6574606 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/71777/1/j.1754-4505.1983.tb01615.x.pdf | |
dc.identifier.doi | 10.1111/j.1754-4505.1983.tb01615.x | en_US |
dc.identifier.source | Special Care in Dentistry | en_US |
dc.identifier.citedreference | Ballschmiede, G. Beitragzurkasuistik der zahnanomalien in bezug auf zahl und grosse. Inang Diss Griefswald, 1922 H 50, 1922, p 751. | en_US |
dc.identifier.citedreference | Rushton, M.A. A case of dentinal dysplasia. Guys Hosp Rep 89: 369 – 373, 1939. | en_US |
dc.identifier.citedreference | Hossins, G.S., and Marsland, E.A. Developmental abnormalities of the dentine and pulp associated with calcinosis. Br Dent J92 ( 12 ): 305 – 311, 1952. | en_US |
dc.identifier.citedreference | Barabas, G.M. The Ehlers-Danlos syndrome. Abnormalities of the enamel, dentine, cementum and the dental pulp: an histological examination of 13 teeth from 6 patients. Br Dent J 126 ( 11 ): 509 – 515, 1969. | en_US |
dc.identifier.citedreference | Elsahy, N.I., and Waters, R.W. The brachio-skeleto-genital syndrome: a new hereditary syndrome. Plast Reconstr Surg 48 ( 6 ): 542 – 550, 1971. | en_US |
dc.identifier.citedreference | Shields, E.D.; Bixler, D.; and el-Kafrawy, A.M. A proposed classification for heritable human dentine defects with a description of a new entity. Arch Oral Biol 18 ( 4 ): 543 – 553, 1973. | en_US |
dc.identifier.citedreference | Morris, M.E., and Augsburger, R.H. Dentine dysplasia with sclerotic bone and skeletal anomalies inherited as an autosomal dominant trait: a new syndrome. Oral Surg 43 ( 2 ): 267 – 283, 1977. | en_US |
dc.identifier.citedreference | Eastman, J.R.; Melnick, M.; and Goldblatt. L.I. Focal odontoblastic dysplasia: dentin dysplasia type III? Oral Surg 44 ( 6 ): 909 – 914, 1977. | en_US |
dc.identifier.citedreference | Witkop, C.J., Jr. Hereditary defects of dentin. In Poole, A.E., ed. Genetics of North America. Philadelphia, W. B. Saunders Co, 1975, pp 25 – 45. | en_US |
dc.identifier.citedreference | Melnick, M.; Levin, L.S.; and Brady, J. Dentin dysplasia: a type 1: a scanning electron microscopic analysis of the primary dentition. Oral Surg 50 ( 4 ): 335 – 340, 1980. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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