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Quoted phrase not found in phrase index: "Abnormality of mouth shape"
Page 1
Dental and oral anomalies in incontinentia pigmenti: a systematic review.
Minić S, Trpinac D, Gabriel H, Gencik M, Obradović M. Minić S, et al. Clin Oral Investig. 2013 Jan;17(1):1-8. doi: 10.1007/s00784-012-0721-5. Epub 2012 Mar 28. Clin Oral Investig. 2013. PMID: 22453515 Review.
Most of the anomaly types were dental, and the most frequent of these were dental shape anomalies, hypodontia, and delayed dentition. The most frequent oral anomaly types were cleft palate and high arched palate. ...
Most of the anomaly types were dental, and the most frequent of these were dental shape anomalies, hypodontia, and delayed dentition. …
Association between Dental Anomalies and Orofacial Clefts: A Meta-analysis.
Marzouk T, Alves IL, Wong CL, DeLucia L, McKinney CM, Pendleton C, Howe BJ, Marazita ML, Peter TK, Kopycka-Kedzierawski DT, Morrison CS, Malmstrom H, Wang H, Shope ET. Marzouk T, et al. JDR Clin Trans Res. 2021 Oct;6(4):368-381. doi: 10.1177/2380084420964795. Epub 2020 Oct 8. JDR Clin Trans Res. 2021. PMID: 33030085 Free PMC article.
The meta-analysis revealed statistically significant associations between OC and agenesis (OR, 14.2; 95% CI, 9.4 to 21.3), supernumerary teeth (OR, 5.7; 95% CI, 3.3 to 9.7), developmental enamel defects (OR, 5.6; 95% CI, 3.5 to 9.0), microdontia (OR, 14.8; 95% CI, 4.0 to 54.6), p …
The meta-analysis revealed statistically significant associations between OC and agenesis (OR, 14.2; 95% CI, 9.4 to 21.3), supernumerary tee …
Atypical Radicular Anatomy in Permanent Human Teeth: A Systematic Review.
Nino-Barrera J, Alzate-Mendoza D, Olaya-Abril C, Gamboa-Martinez LF, Guamán-Laverde M, Lagos-Rosero N, Romero-Diaz AC, Duran N, Vanegas-Hoyose L. Nino-Barrera J, et al. Crit Rev Biomed Eng. 2022;50(1):19-34. doi: 10.1615/CritRevBiomedEng.2022043742. Crit Rev Biomed Eng. 2022. PMID: 35997108
We found that the mandibular first premolar had the highest prevalence of C-shaped canals. Dens invaginatus was more frequently found in the mandibular lateral incisor. ...The classifications systems used in this review allowed for the better understanding and analysis of …
We found that the mandibular first premolar had the highest prevalence of C-shaped canals. Dens invaginatus was more frequently found …
Dental Manifestations of Ehlers-Danlos Syndromes: A Systematic Review.
Kapferer-Seebacher I, Schnabl D, Zschocke J, Pope FM. Kapferer-Seebacher I, et al. Acta Derm Venereol. 2020 Mar 25;100(7):adv00092. doi: 10.2340/00015555-3428. Acta Derm Venereol. 2020. PMID: 32147746 Free PMC article.
The main dental features listed in classical EDS were pulp calcification and localized root hypoplasia. Common dental abnormalities observed in vascular EDS were pulp shape modifications (52.2%), exceeding root length (34.8%), and molar root fusion (47.8%). ...
The main dental features listed in classical EDS were pulp calcification and localized root hypoplasia. Common dental abnormalities o …
No consistent association found between dental caries and body mass index in children.
Carson SJ. Carson SJ. Evid Based Dent. 2018 Jun;19(2):38-39. doi: 10.1038/sj.ebd.6401299. Evid Based Dent. 2018. PMID: 29930361
The weighted mean differences and corresponding 95% confidence intervals for dental caries between children with abnormal weight and those with normal weight were analysed.ResultsFourteen cross-sectional studies including 43,860 children (boys: 23,299; girls: 20,561) were …
The weighted mean differences and corresponding 95% confidence intervals for dental caries between children with abnormal weight and …
Chromosome 6p25 deletion syndrome: A case report and review of ophthalmic features.
Le H, Jin E, Jewell A, Jackson-Cook C, Haskell GT, Couser N. Le H, et al. Am J Med Genet A. 2023 Jun;191(6):1639-1645. doi: 10.1002/ajmg.a.63186. Epub 2023 Mar 20. Am J Med Genet A. 2023. PMID: 36941760
The 6p25 deletion syndrome is a rare genetic disorder characterized by a wide spectrum of congenital anomalies. Ophthalmic abnormalities appear to be highly associated with the syndrome, although this relationship has not been well characterized to date. We conducte …
The 6p25 deletion syndrome is a rare genetic disorder characterized by a wide spectrum of congenital anomalies. Ophthalmic abnorma …