Abstract
Introduction: Thalassemia can be classified into alpha and beta depending on the reduced synthesis of alpha or beta chains present in hemoglobin (Hb),1 that results in reduced hemoglobin in body than normal. Aims: Aims at signifing the importance of timely dental treatment in Beta thalassemia patients. Case Report: Here we present a known case of beta thalassemia minor requiring a full mouth rehabilitation treatment performed dental chair-side. Discussion: Thalassemia minor patients inherit only a single beta-globin mutation and have a mild anemia.2 The evaluated predominance of β-thalassemia minor (carriers) in India is 3-8%, which transforms to 35-45 million carriers in 1.3 billion diverse population with culturally and linguistically multi-ethnic people.3. Conclusion: Several ethnic groups have a much higher prevalence of 4–17%.4 The Beta thalassemia minor cases usually go undetected and are often observed in tests for dental treatment or post-dental treatment.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: International Journal of Current Research and Review
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.