법랑질 형성 부전증에 관한 증례 보고
AMELOGENESIS IMPERFECTA : REPORT OF CASE
소속 상세정보
김재곤/Jae-Gon Kim
이영수/허선/박종하/백병주/Young-Su Lee/Sun Her/Jong-Ha Park/Byeong-Ju Baik
KMID : 0358919980250030598
Abstract
요약
본병원 소아치과에 내원한 유치와 영구치 모두에 법랑질 형성 부전증을 가지고 있는 환자
에 대해 교합면의 마모를 방지하여 교합고경을 유지하기 위해 유구치부 stainless steel
crown 및 맹출 중인 제 1 대구치에 sealant, 전치아에 걸쳐서 주기적인 불소도포를 이용해
치료하여 양호한 결과를 얻었다.
#초록#
Amelogenesis imperfecta is a group of hereditary defects of enamel unassociated with
anyother generalized defects. The prevalence of this condition has been estimated to
range from 1 in 14,000 to 1 in 16,000, depending on the population studied. It may be
differentiated into three general types : hypoplastic, hypocalcified, and hypomaturation,
depending on the clinical presentation of the defects and the likely stage of enamel
formation that is primarily affected. The dentin and root form are usually normal, but
the enamel may lack the normal prismatic structure, being laminated throughout its
thickness or at the periphery, with the result that these teeth are more resistant to
decay. This case is that of an sirs-year-old girl brought to the pediatric dentistry
department by her parents for esthetic reasons and also because of slight dental
sensitivity. Clinical and radiographic examinations confirmed amelogenesis imperfecta.
The author has treated with the crowning of the primary molars, using preformed NiCr
crowns and periodic fluoride application on whole dentition.
키워드
amelogenesis imperfecta; hereditary defects; hypocalcified; hypomaturation; hypoplastic;
원문 및 링크아웃 정보
등재저널 정보