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成骨不全症和牙本质生成不全症中发育异常牙本质的评估。

Assessment of dysplastic dentin in osteogenesis imperfecta and dentinogenesis imperfecta.

作者信息

Malmgren Barbro, Lindskog Sven

机构信息

Department of Pediatrics, Pediatric Endocrine Research Unit, B62, Huddinge University Hospital, Karolinska Institutet, Stockholm, Sweden.

出版信息

Acta Odontol Scand. 2003 Apr;61(2):72-80. doi: 10.1080/00016350310001398.


DOI:10.1080/00016350310001398
PMID:12790503
Abstract

Two semiquantitative scoring systems, Clinical Radiographic Score (CRS) and Dysplastic Dentin Score (DDS), were introduced for analyzing degree of dysplastic manifestations in dentin. The utility of both systems was demonstrated in a large material of teeth from patients with dentinogenesis imperfecta (DI) and osteogenesis imperfecta (OI). Twenty teeth from healthy controls, 81 teeth from 40 patients with OI, and 18 teeth with DI without OI (DI type II) were examined. The degree of dysplasia was correlated with type and form of OI and type of DI. The median DDS did not differ between DI associated with OI (DI type I) and DI type II. DDS in OI patients without clinical signs of DI was above that of control teeth. Both circumpulpal and mantle dentin showed increased DDS, although circumpulpal dentin was more severely affected. The median DDS was highest for the most severe type of non-lethal OI (type III). DDS increased significantly with form (severity) of OI. A significant association between DDS and CRS was found, although diagnosis of DI in less severe cases was not possible based on radiographic or clinical signs alone. Thus, the DDS system proved valuable when the CRS system based on radiographic/clinical manifestations failed, the most significant finding being subclinical histological manifestations of DI in patients with OI but without clinical or radiographic signs of DI. These subtle dysplastic changes are most likely an expression of genetic disturbances associated with OI and should not be diagnosed as DI, but rather be termed histologic manifestations of dysplastic dentin associated with OI.

摘要

引入了两种半定量评分系统,即临床放射学评分(CRS)和发育异常牙本质评分(DDS),用于分析牙本质发育异常表现的程度。在大量来自牙本质发育不全(DI)和成骨不全(OI)患者的牙齿材料中证实了这两种系统的实用性。检查了20颗来自健康对照者的牙齿、40例OI患者的81颗牙齿以及18颗无OI的DI牙齿(II型DI)。发育异常的程度与OI的类型和形式以及DI的类型相关。与OI相关的DI(I型DI)和II型DI之间的DDS中位数没有差异。无DI临床体征的OI患者的DDS高于对照牙齿。尽管髓周牙本质受影响更严重,但髓周牙本质和罩牙本质的DDS均升高。最严重的非致死性OI(III型)的DDS中位数最高。DDS随着OI的形式(严重程度)显著增加。发现DDS与CRS之间存在显著关联,尽管仅根据放射学或临床体征无法诊断较轻病例中的DI。因此,当基于放射学/临床表现的CRS系统失效时,DDS系统被证明是有价值的,最显著的发现是OI患者中存在DI的亚临床组织学表现,但无DI的临床或放射学体征。这些细微的发育异常变化很可能是与OI相关的基因紊乱的表现,不应诊断为DI,而应称为与OI相关的发育异常牙本质的组织学表现。

相似文献

[1]
Assessment of dysplastic dentin in osteogenesis imperfecta and dentinogenesis imperfecta.

Acta Odontol Scand. 2003-4

[2]
Dental findings in osteogenesis imperfecta: I. Occurrence and expression of type I dentinogenesis imperfecta.

J Craniofac Genet Dev Biol. 1987

[3]
Dentinogenesis imperfecta in children with osteogenesis imperfecta: a clinical and ultrastructural study.

Int J Paediatr Dent. 2010-3

[4]
Immunoreactivity of tenascin-C in dentin matrix in dentinogenesis imperfecta associated with osteogenesis imperfecta.

J Dent Res. 1996-1

[5]
Hyperfibers and vesicles in dentin matrix in dentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI).

J Oral Pathol Med. 1994-10

[6]
Mild forms of dentinogenesis imperfecta in association with osteogenesis imperfecta as characterized by light and transmission electron microscopy.

J Oral Pathol Med. 1996-5

[7]
Dentinogenesis imperfecta associated with osteogenesis imperfecta: report of two cases.

Chang Gung Med J. 2003-2

[8]
Dental findings in osteogenesis imperfecta: II. Dysplastic and other developmental defects.

J Craniofac Genet Dev Biol. 1987

[9]
ED-A region-containing isoform of cellular fibronectin is present in dentin matrix in dentinogenesis imperfecta associated with osteogenesis imperfecta.

J Dent Res. 1994-6

[10]
Unusual dentinal changes in dentinogenesis imperfecta associated with osteogenesis imperfecta. A case report.

Oral Surg Oral Med Oral Pathol. 1992-4

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[2]
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[3]
Orofacial Features, Oral Health-Related Quality of Life, and Exposure to Bullying in Osteogenesis Imperfecta: A Cross-Sectional Study.

Children (Basel). 2024-7-26

[4]
A standard set of outcome measures for the comprehensive assessment of oral health and occlusion in individuals with osteogenesis imperfecta.

Orphanet J Rare Dis. 2024-8-13

[5]
Morphological Study of Dental Structure in Dentinogenesis Imperfecta Type I with Scanning Electron Microscopy.

Healthcare (Basel). 2022-8-2

[6]
Osteogenesis Imperfecta: New Perspectives From Clinical and Translational Research.

JBMR Plus. 2019-2-20

[7]
Dentinogenesis imperfecta in Osteogenesis imperfecta type XI in South Africa: a genotype-phenotype correlation.

BDJ Open. 2019-4-11

[8]
The dental perspective on osteogenesis imperfecta in a Danish adult population.

BMC Oral Health. 2018-10-24

[9]
Osteogenesis imperfecta: potential therapeutic approaches.

PeerJ. 2018-8-17

[10]
Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort study.

PLoS One. 2017-5-12

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