Background: Non-syndromic hypodontia is the most common developmental dental anomaly, but there is a paucity of literature on its prevalence and severity in the Indian population.
Aim And Objectives: To estimate the prevalence of non-syndromic hypodontia among adolescent schoolchildren in the southern part of India.
Settings And Design: This cross-sectional study was conducted in 20 schools from two states of southern India, named-Andhra Pradesh and Telangana. A total of 5,458 children in the age-group 13 to 15 years were selected.
Materials And Methods: Clinical examination was carried out to check the absence of a permanent tooth and was confirmed by radiographic findings. The inclusion criterion was children with all the permanent teeth erupted (except third molars) and exclusion criteria were teeth missing due to reasons other than congenital agenesis. A Chi-square test was applied to check the significance.
Results: The total prevalence of hypodontia in the study sample was 1.4%. Girls displayed a higher prevalence value (1.9%) than boys (1.1%). Maxillary lateral incisor was the most commonly congenitally missing tooth, followed by mandibular incisors and mandibular second premolar. Overall, hypodontia with a predominance of unilateral pattern and a predilection for the left side was observed.
Conclusion: The most common missing permanent tooth (except third molars) was the maxillary lateral incisor. Hypodontia was more prevalent in females and had a predominance of unilateral patterns with a predilection toward the left side.
How To Cite This Article: Manasa Devi TL, Dutta B, Dwijendra KS, Prevalence and Pattern of Non-syndromic Hypodontia among Adolescents in Southern Part of India. Int J Clin Pediatr Dent 2021;14(4):492-496.
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http://dx.doi.org/10.5005/jp-journals-10005-1983 | DOI Listing |
Hum Genet
November 2024
Department of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Hua Xi Kou Qiang Yi Xue Za Zhi
October 2024
Dept. of Prosthodontics, School and Hospital of Stomatology, Hebei Medical University, Hebei Key Laboratory of Stomatology, Hebei Clinical Research Center for Oral Diseases, Shijiazhuang 050017, China.
Objectives: This study aimed to identifyPAX9variants in non-syndromic tooth agenesis families of China, as well as to analyze the genotype⁃phenotype of non-syndromic tooth agenesis caused by PAX9variants, which can provide a basis for the genetic diagnosis of tooth agenesis.
Methods: We collected the data of 44 patients with non-syndromic oligodontia who underwent treatment at Stomatological Hospital of Hebei Medical University between 2018 and 2023. Whole-exome sequencing was performed on the peripheral blood of the proband and its core family members, and the variants were verified by Sanger sequencing.
Cleft Palate Craniofac J
September 2024
Cleft Palate and Craniofacial Centre, Department of Plastic Surgery, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Objective: Vascular anomalies are often associated with hypertrophy and asymmetry of soft tissues and bony structures. The aim of this retrospective cross-sectional radiographic study was to evaluate dental maturation and development in patients with facial vascular anomalies and congenital infiltrating lipomatosis.
Design: A sample of 342 patients with different vascular anomalies or congenital infiltrating lipomatosis involving the head and neck area was narrowed down to 31 patients with dental panoramic radiographs taken in the mixed dentition.
Prog Orthod
August 2024
Department of Information Technology, College of Computer Science, King Saud University, Riyadh, Saudi Arabia.
BMC Oral Health
August 2024
Division of Pediatric Dentistry, Department of Preventive Dentistry, Faculty of Dentistry, Khon Kaen University, Khon Kaen, Thailand.
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