International Arab Journal of Dentistry
Abstract
Introduction: Sickle cell anemia, a hereditary disease, results from a mutation in the β-globin coding gene that makes up hemoglobin, leading to the deformation of erythrocytes. Numerous oral manifestations result from this disease; however, some may not be specific.
Objectives: This study’s objective is to recognize these clinical manifestations of the disease to be able to manage oral health in sickle cell anemia patients.
Methods: this integrative review analyzes scientific literature on the impact of sickle cell anemia on oral cavity. A bibliographic search was performed in PubMed, ScienceDirect, CINAHL Plus (via EBSCO host), Web of Science and Google Scholar databases using several combined keywords. The research question was: “What is the impact of sickle cell anemia on the oral cavity and dental treatments?”.
Results: By applying the inclusion and exclusion criteria, 11 articles were included in this review.
Conclusions: Studies show that the most common oral manifestations in these patients are periodontal disease and caries, although this association is not well understood.
Recommended Citation
Leal, Fernanda; Guimarães, Maria Inês; Natbeth, Ambre; and Lopes Cardoso, Inês
(2025)
"Sickle Cell Anemia and Its Impact on the Oral Cavity: Integrative Review,"
International Arab Journal of Dentistry: Vol. 16:
Iss.
2, Article 14.
DOI: https://doi.org/10.70174/iajd.v16i2.1491
Available at:
https://e-journals.usj.edu.lb/iajd/vol16/iss2/14
Included in
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Commons, Other Dentistry Commons
