DENTİNOGENESİS İMPERFEKTA TİP I BİR OLGUDA KONSERVATİF VE PROTETİK TEDAVİ YAKLAŞIMLARI (VAKA RAPORU)
Abstract
Keywords
References
- Aplin HM, Hirst KL, Dixon MJ. Refinement of the dentinogenesis imperfecta type II locus to an inter- val of less than 2 centimorgans at chromosome 4q21 and the creation of a yeast artificial chromo- some contig of the critical region. J Dent Res 1999; 78:1270-1276.
- Witkop CJ. Hereditary defects in enamel and dentin. Acta Genet Stat Med 1957: 7:236-239.
- Shields ED, Bixter D, El-Kafrawy AM. Proposal classification for heritable human dentin defects with a description of new entity. Arch Oral Biol 1973; 18: 543-553.
- Shafer WG, Hine MK, Levy BM. A Textbook of Oral Patology. WB Sounders Co, London; 1983: 58-63.
- Tagaki Y, Sasaki S. A probable common disturbance in the early stage of odontoblast differentiation in dentinogenesis imperfecta type I and type II. J Oral Pathol 1988; 17: 208-212
- Suzuki S, Nakata M, Eto K. Clinical nad histologi- cal observation opalescent dentine associated with enamel defects.Oral Surg Oral Med Oral Path 1977; 44: 767-774.
- Butler WT.Dentin matrix problems. Eur J Oral Sci 1998 ; 106:204-210
- Sapir S, Shapira J. Dentinogenesis imperfecta: an early treatment strategy. Pediatr Dent 2001; 23: 232-237.
Details
Primary Language
Turkish
Subjects
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Journal Section
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Authors
Doç. Dr. Yusuf Ziya Bayındır
This is me
Doç. Dr. Funda Bayındır
This is me
Prof. Dr. Nilgün Seven
This is me
Publication Date
March 1, 2005
Submission Date
April 21, 2014
Acceptance Date
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Published in Issue
Year 2005 Volume: 2005 Number: 3