Journals / Ankara Üniversitesi Diş Hekimliği Fakültesi Dergisi / 2003 / Cilt: 30 - Sayı: 1

Hypocalcification type amelogenesis imperfecta: (A case report)

Hipokalsifiye tip amelogenezis imperfekta: Bir olgu nedeniyle

Pages
83–89
Publication Date
2022-10-10
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The erupted incisor teeth restored with direct composite veneer technique and the patient has been followed up routine clinic control.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Amelogenesis imperfecta is an inherited disorder associated with defective ameloblasts.
📊
Key Findings & Data:The prevalence of this condition has been estimated to range from 1 in 718,1 in 16000, depending on population studied.
💡
Conclusion & Impact:The erupted incisor teeth restored with direct composite veneer technique and the patient has been followed up routine clinic control.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Amelogenesis imperfecta is an inherited disorder associated with defective ameloblasts. The prevalence of this condition has been estimated to range from 1 in 718,1 in 16000, depending on population studied. It may be differentiated into three main groups: hypoplastic, hypocalcified and hypomature, depending on the clinical presentation of the defects and the likely stage of enamel formation that is primarily affected. Amelogenesis İmperfecta carries a high morbidity; its sufferers frequently present with sensitive, discolered teeth and decreased lower facial heigh. The aim of this case report was to present the temporaray emergency treatment of a patient diagnosed with amelogenesis imperfekta in mixed dentition who also had complains about sensitivity end esthetics. According to treatment plan, first primary molar teeth restorated with stainless steel crowns to reduce sensitivity and meanwhile the occlusion was increased 2 mm to develop the vertical dimension. The erupted incisor teeth restored with direct composite veneer technique and the patient has been followed up routine clinic control.

Özet

Amelogenezis imperfekta ameloblastlardaki hasarla karakterize kalıtımsal bir hastalıktır. Farklı toplum çalışmalarında 1/718'den, 1/16000'e kadar değişen farklı prévalons değerleri bildirilmiştir. Amelogenezis imperfekta, defektlerin klinik görünümlerine ve mine formasyonun etkilendiği döneme göre; hipoplastik, hipökalsifiye ve de hipomature şeklinde üç esas gruba ayrılır. Yüksek morbi-diteye sahip olan hastalık dişlerde hassasiyet, renklenme ve alt yüz yüksekliğinde azalma ile karakterizedir. Bu olgu raporunun amacı; dişlerinde hassasiyet ve estetik şikayeti ile kliniğimize başvuran ve amelogenezis imperfekta tanısı konulan erken karışık dişlenme dönemindeki bir hastanın geçici acil tedavi prosedürünü sunmaktır. Öncelikle hassasiyeti azaltmak ve vertikal boyutu yükseltmek için yapılan tedavi planlamasına göre; süt molar dişler paslanmaz çelik kuronlarla restore edildi ve bu sırada oklüzyon 2 mm yükseltildi. Estetiği geliştirmek amacı ile de sürmesini tamamlamış keser dişler direkt kompozit veneer tekniği ile restore edilip, hasta rutin klinik takiplere alındı.

🔖

Cite This Article

TUNÇ, Ş. E., SARI, Ş. (2022). Hypocalcification type amelogenesis imperfecta: (A case report). Ankara Üniversitesi Diş Hekimliği Fakültesi Dergisi, Cilt: 30 - Sayı: 1, 83–89. https://ajindex.com/articles/442237

References (15)

  1. Bouvier D, Duprez JP, Pirel C, Vincent B. Amelogenezis imperfekta-a prosthetic rehabilitation: A clinicial report. J Prosthet Dent 1999; 82: 130-1
  2. Brennan MT, O'Connell BC, Rams TE, O'Connell A. Management of gingival over- growth with generalized enamel defects in a child. J Clin Pediatr Dent 1999; 23: 97-101
  3. Atasu M, Biren S, Mumcu G. Hypocalcification type amelogenezis imperfekta in permanent dentition in association with heavily worn primary teeth, gingival hyperplasia, hypodontia and impacted teeth J Clin Pediatr Dent 1999; 23: 117-21
  4. Ooya K, Nalbandian J, Noikura T. Autosomal recessive rough hypoplastic amelogenezis imperfekta. Oral Surg Oral Med Oral Pathol 1988; 65: 449-58
  5. Finn SB. Hereditray opalescent dentition. I. An analysis of the literature on hereditary anomalies of tooth color. In: Greenfield R, Iacona V, ZoveS, BaerP. Periodontal and prosthodontic treatment of amelogenezis imperfecta: A clinical report. J Prosthet Dent 1992; 68: 572-4
  6. Backman B, Holm AK. Amelogenezis imperfecta: prevalence and incidence in a northern Swedish country. Community Dent Oral Epidemiol 1986; 14:43-7
  7. Chosack A, Eidelman E, Wisotski J.Amelogenezis imperfecta among Israeli Jews and description of a new type of local hypoplastic autosomal recesive amelogenezis imperfecta. Oral Surg 1979; 47: 148-56
  8. Witkop CJ. Hereditary defects in enamel and dentin. In: Seow K. Enamel hypoplasia in the primary dentition: a review.ASDC J Dent Child 1991; 58: 441-52
  9. Koray F, Soyman M, Erdoğan G. Investigation of aetiopathogenesis of amelogenezis imperfecta through microscopic, submicroscopic and cytogenic methods; a case reports. J Oral Rehabil 1988; 15: 149-62
  10. Witkop CJ Jr. Amelogenezis imperfecta, dentinogenesis imfperfecta and dentin dysplasia revisited: problems in classification. J Oral Pathol 1988; 17: 547-53
  11. Rada R, Hasiasakos PS. Current treatment modalites in the conservative restoration of amelogenezis imperfecta: a case report. Quintessence Int 1990; 21: 937-42
  12. Kim Seow W. Enamel hypoplasia in the primary dentition: a review. ASDC J Dent Child 1991; 58: 441-52
  13. Kim Seow. Clinical diagnosis and management strategies of amelogenezis imperfecta variants. Pediatr Dent 1993; 15: 384-93
  14. Kim Seow. Dental development in amelogenezis imperfecta: a controlled study. Pediatr Dent 1995; 17: 26-30
  15. Hunter L, Stone D. Supraoccluding cobalt-chrome onlays in the management amelogenezis imperfecta in children; A 2-year case repo