There are few published studies that report the prevalence of intraoral anomalies for young children. The purpose of this study was to investigate the prevalence and distribution of several congenital oral and paraoral anomalies in Taiwanese children under age six. Twenty-five cities and townships were randomly sampled in different areas of Taiwan using the stratified method. These cities and townships represent cross-sectional samples of geographic locations and socioeconomic levels. A total of 981 Taiwanese children under age six were examined with dental mirrors and explorers as part of the national dental survey. The results of this survey indicated an 11.31% prevalence of geographic tongue. This number is higher than that reported in studies previously performed in different countries. The occurrence of double teeth in primary dentition was found to be 2.14%. Ankyloglossia had a frequency of 1.22%, and primary talon cusp a frequency of 0.61%. Seven (0.71%) children exhibited fissured tongues. Thirteen (1.33%) cases of hypodontia were found. These values were different from those reported in several other countries, which may be attributed to differences in the ethnic and racial composition of the population studied.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387978PMC
http://dx.doi.org/10.1155/2020/2056340DOI Listing

Publication Analysis

Top Keywords

taiwanese children
12
children age
12
anomalies taiwanese
8
national dental
8
dental survey
8
cities townships
8
children
5
clinical orodental
4
orodental anomalies
4
age study
4

Similar Publications

This study descried the experiences of fathers who had lost a child to cancer. The participants were eight fathers whose children died following cancer treatment. Semi-structured interviews were conducted, and content analysis identified six major themes: (1) accompanying their child on the final journey home, (2) stabilizing family life, (3) coping with unbearable grief, 4) maintaining the memory and continuing the bond, (5) reflecting on the regrets and contradictions of the treatment process, (6) finding new meaning, and cherishing the present.

View Article and Find Full Text PDF

Word-of-mouth referrals between patients are a critical component of medical tourism for pediatric hematopoietic cell transplantation.

Medicine (Baltimore)

January 2025

Division of Hematology/Oncology, Department of Pediatrics, Chang Gung Memorial Hospital, Chang Gung University, Taoyuan, Taiwan.

The increasing popularity of medical tourism has sparked interest from policymakers, researchers, and the media. Factors influencing medical tourism include service quality, availability, economics, and cultural differences. This study aims to analyze the key factors that influence destination selection for medical tourists.

View Article and Find Full Text PDF

Background: Bone age (BA) and sexual maturity rating (SMR) are crucial measures in assessing adolescent growth and development. However, studies specifically focusing on the association between BA and SMR in the Taiwanese adolescent population are limited. This study aims to utilize AI-assessed BA results to establish a relationship between BA and SMR in the Taiwanese adolescent population, particularly regarding the initiation of puberty.

View Article and Find Full Text PDF

This study aimed to explore the nature of contextual differences in child-parent attachment relationships and examine how these experiences relate to children's psychological outcomes. A theoretically informed qualitative study was conducted using semi-structured interviews with 15 participants across four groups of Taiwanese youths and parents, representing different contextual attachment combinations. Data were analyzed using a hybrid thematic analysis approach, integrating both inductive and deductive methods.

View Article and Find Full Text PDF
Article Synopsis
  • Lesch-Nyhan syndrome (LNS) is a rare genetic disorder caused by HPRT deficiency, and early diagnosis is key to effective management.
  • Three Taiwanese patients were studied to highlight early clinical signs like hyperuricemia and developmental delays, with exome sequencing confirming diagnoses.
  • Findings showed common symptoms in all patients, and early genetic testing could lead to better outcomes by identifying the syndrome before severe manifestations develop.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!