Dental anomalies in pediatric patients with familial adenomatous polyposis

被引:0
作者
Seth Septer
Brenda Bohaty
Robin Onikul
Vandana Kumar
Karen B. Williams
Thomas M. Attard
Craig A. Friesen
Lynn Roosa Friesen
机构
[1] Children’s Mercy Kansas City,Division of Gastroenterology, Hepatology and Nutrition
[2] University of Missouri – Kansas City School of Dentistry,Department of Paediatric Dentistry
[3] Children’s Mercy Kansas City,Department of Dentistry
[4] University of Missouri – Kansas City School of Dentistry,Department of Oral Pathology, Medicine and Oral Radiology
[5] University of Missouri – Kansas City School of Medicine,Department of Biomedical and Health Informatics
[6] University of Missouri – Kansas City School of Dentistry,Department of Corporate Clinical Research & Department of Research and Graduate Programs
来源
Familial Cancer | 2018年 / 17卷
关键词
Familial adenomatous polyposis; Adenomatous polyposis coli gene; Colorectal carcinoma; Osteomas; Dental anomalies; FAP;
D O I
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学科分类号
摘要
Familial adenomatous polyposis patients often present with non-malignant extra-intestinal manifestations which include dental anomalies that may be evident prior to the appearance of the colonic adenomas. The aims of this study were to describe the prevalence and type of dental anomalies and the relationships between gene mutations and dental anomalies in these patients. Twenty-two pediatric familial adenomatous polyposis patients and 46 controls, who were age and gender matched participated. Familial adenomatous polyposis patient’s had a dental examination with panoramic radiograph and medical record review for age at diagnosis, the presence of the adenomatous polyposis coli gene mutation, and determination of other extra-intestinal manifestations on the body. The control group was identified from a retrospective chart review and selected if there was a current panoramic radiograph. The only significant difference between familial adenomatous polyposis patients and controls were the presence of jaw osteomas and sclerosis (p = .0001). Patients with a mutation in, or upstream of codon 1309 had a higher frequency of osteomas (77.8%) and jaw-bone sclerosis (44.4%), and 77% of these had at least one dental anomaly. This preliminary study showed an association between a genetic variant at, or upstream of codon 1309, and radiographic dental anomalies.
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页码:229 / 234
页数:5
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