International Journal of Clinical Pediatric Dentistry

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VOLUME 14 , ISSUE 1 ( January-February, 2021 ) > List of Articles

RESEARCH ARTICLE

Dermatoglyphics: A Noninvasive Diagnostic Tool in Predicting Class III Skeletal Malocclusion in Children

Ashwitha C Belludi, Arvind Sridhara, Narayana Chandra Kumar, Sunil Raj Noojadi

Citation Information : Belludi AC, Sridhara A, Kumar NC, Noojadi SR. Dermatoglyphics: A Noninvasive Diagnostic Tool in Predicting Class III Skeletal Malocclusion in Children. Int J Clin Pediatr Dent 2021; 14 (1):63-69.

DOI: 10.5005/jp-journals-10005-1934

License: CC BY-NC 4.0

Published Online: 14-07-2021

Copyright Statement:  Copyright © 2021; The Author(s).


Abstract

Background: Dermatoglyphics is a scientific study that deals with the epidermal ridges and their configurations on certain body parts such as fingers, palms, and soles. In humans, during the intrauterine life (IUL) the primary palate, lip, and dermal ridges are formed during the same period, the genetic code engineered in the genome normal or abnormal is mirrored on these developing structures. Thus making dermatoglyphic a preceding tool in dental diagnosis. Aims and objectives: The study aimed at evaluating dermatoglyphics as a tool in diagnosing malocclusion by comparing qualitative and quantitative dermal patterns in class I and class III skeletal malocclusion. Materials and methods: Sixty subjects fulfilling inclusion-criteria were segregated into two groups, group I (class I skeletal malocclusion) and group II (class III skeletal malocclusion) with 30 subjects in each group. Dermatoglyphic patterns were recorded using ink method following rolling impression technique on recording sheets. The dermatoglyphic data were assessed for different finger ridge patterns, total finger ridge count, a–b ridge count, and atd angle. Results: The data were analyzed using Chi-square and paired t tests. In skeletal class III malocclusion, there was an increase in loop count and a decrease in the count of whorls and arches as compared to class I malocclusion (p = 0.037). However, in relation to total finger ridge count, a–b ridge count, and atd angle, there was no statistically significant difference found between the groups. Conclusion: The end of the study derived that the fingerprint patterns are valuable and ineradicable markers of malocclusion. Thus, the dermatoglyphics can be utilized as a screening tool for early prediction of skeletal class III malocclusion at a younger age-group. Further studies are suggested with the inclusion of other parameters using the inkless biometric method in different populations.


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  1. Cummins H, Midlo C. Palmar and planter epidermal configuration (dermatoglyphics) in European. Am J Phys-Anthropol 1926;9(4):471–502. DOI: 10.1002/ajpa.1330090422.
  2. Gibbs RC. Fundamentals of dermatoglyphics. Arch Derm 1967;96(6):721–725. DOI: 10.1001/archderm.1967.01610060115023.
  3. Verbov J. Clinical significance and genetics of epidermal ridges-a review of deramtoglyphics. J Investigat Dermatol 1970;54(4):261–271. DOI: 10.1111/1523-1747.ep12258550.
  4. Bramon E, Walshea M, McDonald C. Dermatoglyphics and schizophrenia: a meta-analysis and investigation of the impact of obstetric complications upon a–b ridge count. Schizophr Res 2005;75(2-3):399–404. DOI: 10.1016/j.schres.2004.08.022.
  5. Saha S, Mc Grath J, Chant D, et al. Directional and fluctuating asymmetry in finger and a-b ridge counts in psychosis: a case-control study. BMC Psychiatry 2003;3(1):1–9. DOI: 10.1186/1471-244X-3-1.
  6. Milicic J, Petkovic B, Bozikov J. Dermatoglyphs of digito-palmar complex in autistic disorder: family analysis. Croat Med J 2003;44(4):469–476.
  7. Natekar PE, DeSouza FM. Fluctuating asymmetry in dermatoglyphics of carcinoma of breast. Indian J Hum Genet 2006;12(2):76–81. DOI: 10.4103/0971-6866.42320.
  8. Edelstein J. Dermatoglyphics and acute lymphocytic leukemia in children. J Pediatr Oncol Nurs 1991;8(1):30–38. DOI: 10.1177/104345429100800106.
  9. Alter M, Schulenberg R. Dermatoglyphics in congenital heart disease. Circulation 1970;XLI(1):49–54. DOI: 10.1161/01.cir.41.1.49.
  10. Ziegler AG, Mathies R, Ziegelmayer G, et al. Dermatoglyphics in type 1 diabetes mellitus. Diabet Med 1993;10(8):720–724. DOI: 10.1111/j.1464-5491.1993.tb00154.x.
  11. Reddy S, Prabhakar AR, Reddy VVS. A dermatoglyphic predictive and comparative study of class I, class II div.1, div.2 and class III malocclusions. J Indian Soc Pedod Prev Dent 1997;15(1):13–19.
  12. Mathew L, Hegde AM, Rai K. Dermatoglyphic peculiarities in children with oral clefts. J Indian Soc Pedod Prev Dent 2005;23(4):179–182. DOI: 10.4103/0970-4388.19005.
  13. Škrinjarić IJ, Bačić M. Hereditary gingival fibromatosis: report on three families and dermatoglyphic analysis. J Periodontal Res 1989;24(5):303–309. DOI: 10.1111/j.1600-0765.1989.tb00874.x.
  14. Atasu M. Dermatoglyphic findings in periodontal diseases. Int J Anthropol 2005;20(12):63–75. DOI: 10.1007/BF02445214.
  15. Sharma A, Somani R. Dermatoglyphic interpretation of dental caries and its correlation to salivary bacteria interactions: an in-vivo study. J Indian Soc Pedod Prev Dent 2009;27(1):17–21. DOI: 10.4103/0970-4388.50811.
  16. Venkatesh E, Bagewadi A, Keluskar V, et al. Palmar dermatoglyphics in oral leukoplakia and oral squamous cell carcinoma patients. J Indian Acad Oral Med Radiol 2008;20(3):94–99. DOI: 10.4103/0972-1363.52774.
  17. Massler M, Frankel J. Prevalence of malocclusion in children aged 14 to 18 years. Am J Orthod 1951;37(10):751–768. DOI: 10.1016/0002-9416(51)90047-4.
  18. Haynes S. The prevalence of malocclusion in English school children aged 11–12 years. Transact Eur Orthod Soc 1970. 89–98.
  19. Thilander Bmyrberg N. The prevalence of malocclusion in Swedish schoolchildren. Eur J Oral Sci 1973;81(1):12–20. DOI: 10.1111/j.1600-0722.1973.tb01489.x.
  20. Mayor P, El-Badrawy H. Maxillary protraction for early orthopaedic correction of class III malocclusion. Pediat Dentis 1993;15:203–207.
  21. Guyer EC, Ellis EE, McNamara JA, et al. Components of class III malocclusion in juveniles and adolescents. Angle Orthod 1986;56(1):7–30. DOI: 10.1043/0003-3219(1986)0562.0.CO;2.
  22. The science of fingerprints. [Washington]: U.S. Dept. of Justice, Federal Bureau of Investigation; 1984.
  23. Rajput S, Shenoy S, Thoke B. Palmar dermatoglyphics versus malocclusion: a pilot study. IJRID 2014;4(6):48–56.
  24. Trehan M, Kapoor DN, Tandon P, et al. Dermatoglyphic study of normal occlusion and malocclusion. J Ind Orthod Soc 2000;33:11–16.
  25. Kharbanda OP, Sharma VP, Gupta DS. Dermatoglyphic evaluation of mandibular prognathism. J Ind Dent Assoc 1982;54(5):179–186.
  26. Uchida JA, Solton HC. Evaluation of dermatoglyphics in medical genetics. Pediatr Clin North Am 1963;10(2):409–422. DOI: 10.1016/S0031-3955(16)31409-2.
  27. Boeck EM, Lunardi N, Pinto AS, et al. Occurrence of skeletal malocclusions in Brazilian patients with dentofacial deformities. Braz Dent J 2011;22(4):340–345. DOI: 10.1590/s0103-644020110004 00014.
  28. Slatis HM, Katznelson MBM, Bonne-Tamir B. The inheritance of fingerprint patterns. Am J Hum Genet 1976;28(3):280–289.
  29. Reddy BRM, Sankar SG, Roy ET, et al. A comparative study of dermatoglyphic in individuals with normal occlusion and malocclusions. J Clin Diagnos Res 2013;7(12):3060–3065. DOI: 10.7860/JCDR/2013/7663.3853.
  30. Eslami N, Jahanbin A, Ezzati A, et al. Can dermatoglyphics be used as a marker for predicting future malocclusions? Elect Phys 2016;8(2):1927–1932. DOI: 10.19082/1927.
  31. Penrose LS, Losch D. The effect of sex chromosome on some characteristics of dermal ridges on palm and finger tips. Genet Pol 1969;10:328.
  32. Holt SB. The hypothenar radial arch, a genetically determined epidermal ridge configuration. Am J Phys Anthropol 1975;42(2):211–214. DOI: 10.1002/ajpa.1330420206.
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