VOLUME 17 , ISSUE 10 ( October, 2024 ) > List of Articles
Swagata Saha, Kripa Dutta, Prajna P Nayak, Manju Raman Nair, Viraj Jayant Naik, Ananya Rao K
Keywords : Case report, Comprehensive health care, Dental care, Developmental disabilities, Genetic disorders, rare, Smith−Magenis syndrome
Citation Information : Saha S, Dutta K, Nayak PP, Nair MR, Naik VJ, K AR. Sugar-coated Sleep: Raising Dental Red Flags in Smith−Magenis Syndrome. Int J Clin Pediatr Dent 2024; 17 (10):1189-1192.
DOI: 10.5005/jp-journals-10005-2968
License: CC BY-NC 4.0
Published Online: 27-11-2024
Copyright Statement: Copyright © 2024; The Author(s).
Aim and background: Smith−Magenis syndrome (SMS) is a rare condition characterized by abnormalities affecting chromosome 17 or RAI1, leading to physical, developmental, and behavioral challenges. SMS occurs in approximately 1 in 25,000 individuals, presenting complex clinical and dental issues. Case description: This case report focuses on the dental care of a 3-year-old child diagnosed with SMS, emphasizing a comprehensive treatment plan. The child exhibited typical SMS traits, including sleep disturbances, developmental delays, and behavioral problems. The multidisciplinary team integrated dental interventions with strategies to manage these challenges effectively. Conclusion: This report contributes to the limited knowledge on managing SMS, highlighting the effectiveness of a multidisciplinary approach in meeting the diverse needs of affected individuals. Clinical significance: The scarcity of literature on SMS underscores the importance of documenting such rare cases to enhance understanding and tailor interventions. By documenting successful management strategies, clinicians can better support patients with this rare disorder.