Prevalence and Distribution of Dental Anomalies among Arab Orthodontic Patients in Israel: Is There a Correlation to Consanguinity Marriage?
Abstract
:1. Introduction
2. Materials and Methods
2.1. Study Sample
2.2. Evaluation Procedure
2.3. Dental Anomalies
2.4. Statistical Analysis
2.5. Reliability
3. Results
3.1. Reliability Analysis
3.2. General Prevalence of Dental Anomalies
3.3. Severity of Dental Anomalies
3.4. Consanguinity
4. Discussion
4.1. Dental Anomalies: General Prevalence, Gender, the Number of Anomalies and the Teeth Involved
4.2. Dental Anomalies and Consanguinity
4.3. Study Limitations
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Altug-Atac, A.T.; Erdem, D. Prevalence and distribution of dental anomalies in orthodontic patients. Am. J. Orthod. Dentofac. Orthop. 2007, 131, 510–514. [Google Scholar] [CrossRef] [PubMed]
- Ansari, G.; Mojtaba, V.G.; Welbury, R. Atlas of Pediatric Oral and Dental Developmental Anomalies. Internet. Resour. 2019, 4, 21–61. [Google Scholar]
- Clayton, J.M. Congenital dental anomalies occurring in 3557 children. J. Dent. Child 1956, 23, 206–218. [Google Scholar]
- Shah, R.M.; Boyd, M.A.; Vakil, T.F. Studies of permanent tooth anomalies in 7,886 Canadian individuals. I: Impacted teeth. Dent. J. 1978, 44, 262–264. [Google Scholar] [PubMed]
- Ooshima, T.; Ishida, R.; Mishima, K.; Sobue, S. The prevalence of developmental anomalies of teeth and their association with tooth size in the primary and permanent dentitions of 1650 Japanese children. Int. J. Paediatr. Dent. 1996, 6, 87–94. [Google Scholar] [CrossRef] [PubMed]
- Thongudomporn, U.; Freer, T.J. Prevalence of dental anomalies in orthodontic patients. Aust. Dent. J. 1998, 43, 395–398. [Google Scholar]
- Shapira, Y.; Blum, I.; Hakali, Z.; Shpack, N.; Amitai, Y. Prevalence of non-syndromic orofacial clefts among Jews and Arabs, by type, site, gender and geography: A multicenter study in Israel. Isr. Med. Assoc. J. 2014, 16, 759–763. [Google Scholar]
- Zlotogora, J. Genetic disorders among Palestinian Arabs. Effect of consanguinity. Am. J. Med. Genet. 1997, 68, 472–475. [Google Scholar] [CrossRef]
- Teebi, A.S. Autosomal recessive disorder among Arabs: An overview from Kuwait. J. Med. Genet. 1994, 38, 163–167. [Google Scholar] [CrossRef] [Green Version]
- Jaber, L.; Bailey-Wilson, J.E.; Hai-Yehia, M.; Hermandez, J.; Shohat, M. Consanguineous mating in an Israeli-Arab community. Arch. Pediatr. Adolesc. Med. 1994, 148, 412–415. [Google Scholar] [CrossRef]
- Al Ansari, A. Etiology of mild mental retardation among Bahraini children: A community-based case control study. Ment. Retard. 1993, 31, 140–143. [Google Scholar] [PubMed]
- Jaber, L.; Merlob, P.; Gabriel, R.; Shohat, M. Effects of consanguineous marriage on reproductive outcome in an Arab community in Israel. J. Med. Genet. 1997, 34, 1000–1002. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Bener, A.; Hussain, R. Consanguineous unions and child health in the State of Qatar. Paediatr. Perinat. Epidemiol. 2006, 20, 372–378. [Google Scholar] [CrossRef] [PubMed]
- Chakraborty, R.; Chakravarti, A. On consanguineous marriages and the genetic load. Hum. Genet. 1977, 36, 47–54. [Google Scholar] [CrossRef] [PubMed]
- Khoury, S.A.; Massad, F. Consanguinity, fertility, reproductive wastage, infant mortality, and congenital malformations in Jordan. Saudi Med. J. 2000, 21, 150–154. [Google Scholar] [PubMed]
- Mokhtar, M.; Abdel Fattah, M.M. Consanguinity and advanced maternal age as risk factors for reproductive losses in Alexandria, Egypt. Eur. J. Epidemiol. 2001, 17, 559–565. [Google Scholar] [CrossRef]
- Zlotogora, J.; Leventhal, A.; Amitai, Y. The impact of congenital malformations and Mendelian diseases on infant mortality in Israel. Isr. Med. Assoc. J. 2003, 5, 416–418. [Google Scholar]
- Bromiker, R.; Glam Baruch, M.; Gofin, R.; Hammerman, C.; Amitai, Y. Association of parental consanguinity with congenital malformation among Arab newborns in Jerusalem. Clin. Genet. 2004, 66, 63–66. [Google Scholar] [CrossRef]
- Sawardekar, K.P. Profile of major congenital malformations at Nizwa Hospital, Oman: 10-year review. J. Pediatr. Child Health 2005, 41, 323–330. [Google Scholar] [CrossRef]
- Harlap, S.; Kleinhaus, K.; Perrin, M.; Calderon-Margalit, R.; Paltiel, O.; Deutsch, L.; Manor, O.; Tiram, E.; Yanetz, R.; Friedlander, Y. Consanguinity and birth defects in the Jerusalem perinatal study cohort. Hum. Hered. 2008, 66, 180–189. [Google Scholar] [CrossRef] [Green Version]
- Al Khabori, M. Causes of severe to profound deafness in Omani paediatric population. Int. J. Pedia. Otorhinolaryngol. 2004, 68, 1307–1313. [Google Scholar] [CrossRef] [PubMed]
- Zlotogora, J.; Carasquillo, M.; Barges, S.; Shalev, S.A.; Hujerat, Y.; Chakravarti, A. High incidence of deafness from three frequent connexin 26 mutations in an isolated community. Genet. Test. 2006, 10, 40–43. [Google Scholar] [CrossRef]
- Bener, A.; Denic, S.; Al Mazrouei, M. Consanguinity and family history of cancer in children with leukemia and lymphomas. Cancer 2001, 92, 1–6. [Google Scholar] [CrossRef] [PubMed]
- Masood Gilani, G.; Kamal, S. Risk factors for breast cancer in Pakistani women aged less than 45 years. Ann. Hum. Biol. 2004, 31, 398–407. [Google Scholar] [CrossRef] [PubMed]
- Barbari, A.; Stephan, A.; Masri, M.; Karam, A.; Aoun, S.; El Nahas, J.; Khalil, J.B. Consanguinity-associated kidney diseases in Lebanon: An epidemiological study. Mol. Immu. 2003, 39, 1109–1114. [Google Scholar] [CrossRef]
- Pasotti, M.; Repetto, A.; Tavazzi, L.; Arbustini, E. Genetic predisposition to heart failure. Medi. Clinz. 2004, 88, 1173–1192. [Google Scholar] [CrossRef]
- Lakshmayya Naidu, D.; Srinivasa Raju, M.; Goel, S. Effects of consanguineous marriages on oral and craniofacial structures: A study on dental patients in north India. Ann. Essences Dent. 2010, 2, 4–199. [Google Scholar] [CrossRef]
- Sharkia, R.; Khatib, M.; Sheikh-Muhammad, A.; Mahajnah, M.; Zalan, A. The prevailing trend of consanguinity in the Arab society of Israel: Is it still a challenge? J. Biosoc. Sci. 2021, 6, 1–5. [Google Scholar] [CrossRef]
- Watted, N.; Abu-Hussein, M.; Awadi, O.; Watted, M.; Watted, A.-L.; Watted, A. Clinical Study Of Impacted Canine In The Arab Population In Israel. J. Oral. Health Comm. Dent. 2015, 9, 81–88. [Google Scholar]
- Abu-Hussein, M.; Watted, N.; Azzaldeen, A.; Yehia, M.; Awadi, O.; Abu-Hussein, Y. Prevalence of missing lateral incisor agenesis in an orthodontic Arabs population in Israel (Arab48). Int. J. Public Health Res. 2015, 3, 101–107. [Google Scholar]
- Israel Central Bureau of Statistics. Population of Israel on the Eve of 2019; Israel Central Bureau of Statistics: Jerusalem, Israel, 2019. [Google Scholar]
- Sella Tunis, T.; Sarne, O.; Hershkovitz, I.; Finkelstein, T.; Pavlidi, A.M.; Shapira, Y.; Davidovitch, M.; Shpack, N. Dental Anomalies’ Characteristics. J. Diagn. 2021, 11, 1161. [Google Scholar] [CrossRef] [PubMed]
- Hua, F.; He, H.; Ngan, P.; Bouzid, W. Prevalence of peg-shaped maxillary permanent lateral incisors: A meta-analysis. Am. J. Orthod. Dentofac. Orthop. 2013, 144, 97–109. [Google Scholar] [CrossRef] [PubMed]
- Finkelstein, T.; Shapira, Y.; Bechor, N.; Shpack, N. Fused and Geminated Permanent Maxillary Central Incisors: Prevalence, Treatment Options, and Outcome in Orthodontic Patients. J. Dent. Child. 2015, 82, 147–152. [Google Scholar]
- Shapira, Y.; Kuftinec, M.M. Tooth transpositions—A review of the literature and treatment considerations. Angle Orthod. 1989, 59, 271–276. [Google Scholar] [PubMed]
- Mazinis, E.; Zafeiriadis, A.; Karathanasis, A.; Lambrianidis, T. Transmigration of impacted canines: Prevalence, management and implications on tooth structure and pulp vitality of adjacent teeth. Clin. Oral. Investig. 2012, 16, 625–632. [Google Scholar] [CrossRef]
- Bondemark, L.; Tsiopa, J. Prevalence of ectopic eruption, impaction, retention and diagenesis of the permanent second molar. Angle Orthod. 2007, 77, 773–778. [Google Scholar] [CrossRef] [Green Version]
- Bedoya, M.M.; Park, J.H. A review of the diagnosis and management of impacted maxillary canines. J. Am. Dent. Assoc. 2009, 140, 1485–1493. [Google Scholar] [CrossRef] [Green Version]
- Raghoebar, G.M.; Boering, G.; Vissink, A.; Stegenga, B. Eruption disturbances of permanent molars: A review. J. Oral. Pathol. Med. 1991, 20, 159–166. [Google Scholar] [CrossRef]
- Cabay, R.J. An overview of molecular and genetic alterations in selected benign odontogenic disorders. Arch. Pathol. Lab. Med. 2014, 138, 754–758. [Google Scholar] [CrossRef]
- Aren, G.; Guven, Y.; Guney Tolgay, C.; Ozcan, I.; Bayar, O.F.; Kose, T.E.; Koyuncuoglu, G.; Ak, G. The prevalence of dental anomalies in a Turkish population. J. Istanb. Univ. Fac. Dent. 2015, 49, 23–28. [Google Scholar] [CrossRef] [Green Version]
- Gokcek, M.; Cirakoglu, N.Y. Determination of the prevalence of dental anomalies by digital panoramic radiography analysis. Medicine 2021, 10, 1128–1132. [Google Scholar]
- Guttal, K.S.; Naikmasur, V.G.; Bhargava, P.; Bathi, R.J. Frequency of developmental dental anomalies in the Indian population. Eur. J. Dent. 2010, 4, 263–269. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Bharathi, A.R.; Santhanam, A.; Sivakumar, M. Prevalence of impacted maxillary canines and its association with other dental anomalies. Int. J. Dent. Oral Sci. 2021, 8, 1757–1760. [Google Scholar]
- Bağcı, N.; Pamukçu, U.; Altunkaynak, B.; Peker, İ. Dental anomalies in consanguineous marriage: A clinical-radiological study. Int. Dent. J. 2022, 72, 133–140. [Google Scholar] [CrossRef] [PubMed]
- Khan, S.Y. An exploratory study of consanguinity and dental developmental anomalies. Int. J. Clin. Pediatr. Dent. 2018, 11, 513–518. [Google Scholar] [CrossRef] [PubMed]
- Abbas, B.; Abbas, S.; Malik, S.M.; Rahim, M.; Umair, M.; Khurshid, Z. Consanguineous Marriages and Dental Anomalies: A Cross-Sectional Analytical Study. Int. J. Dent. 2022, 2022, 9750460. [Google Scholar] [CrossRef]
- Basdra, E.K.; Kiokpasoglou, M.; Stellzig, A. The Class II Division 2 craniofacial type is associated with numerous congenital tooth anomalies. Eur. J. Orthod. 2000, 22, 529–535. [Google Scholar] [CrossRef] [Green Version]
- Baydas, B.; Oktay, H.; Metin Dagsuyu, I. The effect of heritability on Bolton tooth-size discrepancy. Eur. J. Orthod. 2005, 27, 98–102. [Google Scholar] [CrossRef] [Green Version]
- Garn, S.M.; Lewis, A.B.; Kerewsky, R.S. X-LINKED inheritance of tooth size. J. Dent. Res. 1965, 44, 439–441. [Google Scholar] [CrossRef]
- Kotsomitis, N.; Dunne, M.P.; Freer, T.J. A genetic etiology for some common dental anomalies: A pilot twin study. Aust. Orthod. J. 1996, 14, 172–178. [Google Scholar]
- Sofaer, J.A. Human tooth-size asymmetry in cleft lip with or without cleft palate. J. Arch. Oral Biol. 1979, 24, 141–146. [Google Scholar] [CrossRef] [PubMed]
- Shapira, Y.; Blum, I.; Haklai, Z.; Shpack, N.; Amitai, Y. Nonsyndromic orofacial clefts among Jews and non-Jews born in 13 hospitals in Israel during 1993–2005. Community Dent. Oral Epidemiol. 2018, 46, 586–591. [Google Scholar] [CrossRef] [PubMed]
Dental Anomaly | Diagnostic Criteria |
---|---|
Missing teeth | Lack of development of one or more permanent teeth. |
Supernumerary teeth | An excess in the normal number of permanent teeth due to the development of additional teeth. |
Peg-shaped teeth | A tooth with an incisor mesio-distal width smaller than its cervical width [33]. |
Fusion | Union between two separate tooth buds during dental development involving the crowns and/or the roots [34]. |
Gemination | Inadequate division of a tooth germ, resulting in the formation of two partially or completely separated crowns with one root and one root canal. It is clinically characterized by incisal notching on an enlarged crown [34]. |
Transposition | Interchange in the position of two adjacent permanent teeth in the same quadrant of the dental arch [35]. |
Transmigration | Movement of an impacted tooth across the jaw midline [36]. |
Ectopic | An erupted tooth that is not in its proper position in the dental arch (e.g., the tooth is located mesially/distally or vestibularlly/orally outside the dental arch [37]. |
Impaction | Interruption in the eruption of a tooth caused by a clinically or radiographically detectable physical barrier in the eruption path, or because of an abnormal position of the tooth [38,39]. |
Submerged | A deciduous erupted tooth that failed to reach the occlusal level of the fully erupted adjacent teeth by at least 2 mm. |
Retained | Failure of the primary tooth to exfoliate at the proper developmental stage (more than one year late to erupt from its permanent successor) [39]. |
Dilacerations | Teeth with bends or changes in the long axis of their crowns, crown-roots, or roots. This is usually following trauma to the developing tooth bud. |
Taurodontism | The furcation areas on the molar teeth are located more epically than normal, and the pulp chamber appears elongated as a result. This anomaly is detected in radiographs and is seen in both dentitions, but is morecommon in the permanent dentition [2]. |
Odontoma | An odontoma is a tumor-like malformation that contains elemental tooth matrix materials [40]. |
Dental Anomaly | Gender | n | Prevalance (%) | p-Value 1 |
---|---|---|---|---|
Missing teeth | Male Female Total | 16 22 38 | 8.2 6.9 7.4 | 0.589 |
Supernumerary teeth | Male Female Total | 1 4 5 | 0.5 1.3 1 | 0.404 |
Peg-shaped teeth | Male Female Total | 2 3 5 | 1 0.9 1 | 0.927 |
Fusion | Male Female Total | 1 0 1 | 0.5 0 0.2 | 0.201 |
Gemination | Male Female Total | 2 0 2 | 1 0 0.4 | 0.700 |
Transmigration | Male Female Total | 0 1 1 | 0 0.3 0.2 | 0.433 |
Ectopic | Male Female Total | 16 14 30 | 8.2 4.4 5.8 | 0.750 |
Impaction | Male Female Total | 38 31 69 | 19.5 9.7 13.5 | 0.002 |
Submerged | Male Female Total | 1 2 3 | 0.5 0.6 0.6 | 0.807 |
Retained | Male Female Total | 6 8 14 | 3.1 2.5 2.7 | 0.705 |
Dilacerations | Male Female Total | 1 1 2 | 0.5 0.3 0.4 | 0.726 |
Taurodontism | Male Female Total | 1 3 4 | 0.5 0.9 0.8 | 0.590 |
Odontoma | Male Female Total | 1 1 2 | 0.5 0.3 0.4 | 0.726 |
With Consanguinity | Without Consanguinity | Total | |
---|---|---|---|
With a dental anomaly | 45 | 105 | 150 |
Without a dental anomaly | 34 | 329 | 363 |
Total | 79 | 434 | 513 |
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Kadry, R.; Atalla, R.; Sella Tunis, T.; Finkelstein, T.; Schonberger, S.; Kharouba, J.; Shapira, Y. Prevalence and Distribution of Dental Anomalies among Arab Orthodontic Patients in Israel: Is There a Correlation to Consanguinity Marriage? Appl. Sci. 2023, 13, 197. https://doi.org/10.3390/app13010197
Kadry R, Atalla R, Sella Tunis T, Finkelstein T, Schonberger S, Kharouba J, Shapira Y. Prevalence and Distribution of Dental Anomalies among Arab Orthodontic Patients in Israel: Is There a Correlation to Consanguinity Marriage? Applied Sciences. 2023; 13(1):197. https://doi.org/10.3390/app13010197
Chicago/Turabian StyleKadry, Rana, Rojee Atalla, Tatiana Sella Tunis, Tamar Finkelstein, Shirley Schonberger, Johnny Kharouba, and Yehoshua Shapira. 2023. "Prevalence and Distribution of Dental Anomalies among Arab Orthodontic Patients in Israel: Is There a Correlation to Consanguinity Marriage?" Applied Sciences 13, no. 1: 197. https://doi.org/10.3390/app13010197
APA StyleKadry, R., Atalla, R., Sella Tunis, T., Finkelstein, T., Schonberger, S., Kharouba, J., & Shapira, Y. (2023). Prevalence and Distribution of Dental Anomalies among Arab Orthodontic Patients in Israel: Is There a Correlation to Consanguinity Marriage? Applied Sciences, 13(1), 197. https://doi.org/10.3390/app13010197