Evaluation of craniofacial anthropometry of children with β-thalassemia major in the eastern Anatolia: a case-control study.

Clin Oral Investig

Department of Pediatric Hematooncology, Department of Medical Sciences Pediatric Health And Diseases, School of Medicine, Acıbadem Mehmet Ali Aydınlar University, Fahrettin Kerim Gökay Caddesi No:49Altunizade / Üsküdar, 34662, Istanbul, Turkey.

Published: October 2023

Objective: The present study aims to compare β-thalassemia major patients and healthy individuals in terms of anthropometric characteristics and changes in craniofacial profile.

Subjects And Method: Craniofacial anthropometric measurements were performed on a total of 422 subjects (199 β-thalassemia major patients and 223 healthy individuals) by using a millimetric caliper and tape measure on 19 anthropometric parameters (8 horizontal, 10 vertical, and 1 head circumference) in cranial, facial, nasal, orolabial, and orbital zones.

Results: The difference between the orbital, nasal, and orolabial zone parameters of healthy subjects and β-thalassemia major patients was found to be statistically significant (p < 0.05). There was no statistically significant difference between the groups in terms of head circumference in the cranial zone and total facial height in facial zone (n-gn) values (p˃0.05). In intragroup comparison between females and males with β-thalassemia, statistically significant differences were found in forehead width (ft-ft), forehead height (tr-gl), right eye width (R ex-ex), and upper lip height (sn-stm) (p < 0.05).

Conclusion: Understanding the craniofacial profile changes in β-thalassemia major patients and increasing our knowledge about the relationship between the course and severity of disease and the level of these changes would contribute to the advancements in diagnoses to be made in facial and jaw zones of these patients and in the treatment plans.

Clinical Relevance: We believe that the analysis and results of the craniofacial anthropometric data obtained in the study will contribute to the diagnosis and treatment processes of patients with β-thalassemia major in areas of expertise such as craniofacial surgery, orthodontics, and hemato-oncology.

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Source
http://dx.doi.org/10.1007/s00784-023-05191-zDOI Listing

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