ŞİDDETLİ HİPODONTİ:DÖRT VAKA RAPORU ve LİTERATÜRÜN ARAŞTIRILMASI

Abstract

-

Keywords

• -

SEVERE HYPODONTIA: FOUR CASE REPORTS AND REVIEW OF THE LITERATURE

Abstract

Di kayb", vücudun genelini etkileyen bir durumun parças" veya lokal bir durum olabilir. Vücudun genelini etkileyen bir durum olarak oligodonti (di lerin k"smi kayb"), ektodermal displazi ile birlikte görülebilir. Di kayb"; tek bir di kayb", birkaç di in kayb" veya anodonti (tüm di lerin kayb") eklinde olabilir. 3. molarlar eksikliBi en s"k görülen durum olup, onu s"ras"yla mandibular 2. molarlar, maksiller lateral kesiciler ve maksiler 2. premolar di ler takip eder. Hem çevresel hem de genetik faktörler di geli iminde bozukluBun olu mas"na sebep olabilir. Fakat vakalar"nçoBunda dihipodonti, otozomal dominant geçi li kal"tsal bir durumdur

Keywords

• Ciddetli hipodonti, Digeli imi, Radyografi, Di anomalisi

References

1. Jernvall J, Thesleff I. Reiterative signalling and patterning during mammalian morphogenesis. Mech Dev 2000; 92: 19-29.
2. Jumlongras D, Bei M, Stimson JM, Wang WF, DePalma SR, Seidman CE, et al. A nonsense mutation in MSX1 causes Witkop Syndrome. Am J Hum Genet 2001; 9: 743-746.
3. Schalk-Van Der Weide Y, Bosman F. Tooth size in relatives of individuals with oligodontia. Arch Oral Biol 1996; 41: 469-472.
4. Dhanrajani PJ. Hypodontia: etiology, clinical features and management. Quintessence Int ; 33: 294–302. Jorgenson RJ. Clinician’s view of hypodontia. JADA 1980: 101: 283–286.
5. Pirinen S, Thesleff I. Development of the dentition. In: Thilander B, Rönning O (eds). Introduction to Orthodontics. Stockholm, 1995: 43.
6. K"rz"oBlu Z, Köseler CT, Ertürk MSÖ, Karay"lmaz H. Clinical features of hypondontia and associated dental anomalies: a retrospective study. Oral Diseases 2005; 11: 399–404.
7. Muller TP, Hill IN, Petreson AC, Blayney JR. A survey of congenitally missing permanent teeth. J Am Dent Assoc 1970; 81: 101–107.
8. Zarrinnia K, Bassiouny MA. Combined aplasia of maxillary first molars and lateral incisors: a case report and management. J Clin Pediatr Dent ; 27: 127–132. tooth Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE. A human MSX 1 homeodomain missense mutation causes selective tooth agenesis. Nat Genet 1996; 13: 417-421.

9. Schalk-van der Weide Y. Oligodontia. A clinical, radiographic and genetic evaluation. Thesis. Utrecht, University of Utrecht, 1992.
10. Ahmad W, Brancolini V, ul Faiyaz MF, Lam H, ul Haque S, Haider M et al. A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1. Am J Hum Genet 1998; 62: 987-991.
11. Pirinen S, Kentala A, Nieminen P, Varilo T, Thesleff I, Arte S. Recessively inherited lower incisor hypodontia. J Med Genet 2001; 38: 551–
12. Corresponding author: M. Akif SÜMBÜLLÜ , DDS phD Address: Department of Oral Diagnosis and Oral Radiology, Faculty of Dentistry, Atatürk University, Erzurum, Turkey Business telephone number: 0090.442.2311765 Fax number: 0090.442.2360945
13. E-mail address: [e-mail] Yaz;,ma Adresi