Saha Swagata, Dutta Kripa, Nayak Prajna Prabhakar, Nair Manju Raman, Naik Viraj Jayant, Rao K Ananya
Department of Pediatric and Preventive Dentistry, AB Shetty Memorial Institute of Dental Sciences (ABSMIDS), NITTE (Deemed to be University), Deralakatte, Mangaluru, Karnataka, India.
Int J Clin Pediatr Dent. 2024 Oct;17(10):1189-1192. doi: 10.5005/jp-journals-10005-2968.
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.
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.
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.
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.
Saha S, Dutta K, Nayak PP, Sugar-coated Sleep: Raising Dental Red Flags in Smith-Magenis Syndrome. Int J Clin Pediatr Dent 2024;17(10):1189-1192.
史密斯-马吉尼斯综合征(SMS)是一种罕见疾病,其特征是影响17号染色体或RAI1基因的异常,导致身体、发育和行为方面的挑战。SMS在大约每25000人中出现1例,会引发复杂的临床和牙科问题。
本病例报告聚焦于一名被诊断患有SMS的3岁儿童的牙科护理,着重介绍了一个全面的治疗方案。该儿童表现出典型的SMS特征,包括睡眠障碍、发育迟缓及行为问题。多学科团队将牙科干预与有效应对这些挑战的策略相结合。
本报告为关于SMS管理的有限知识做出了贡献,突出了多学科方法在满足受影响个体多样化需求方面的有效性。
关于SMS的文献稀缺,这凸显了记录此类罕见病例以增进理解并定制干预措施的重要性。通过记录成功的管理策略,临床医生可以更好地支持患有这种罕见疾病的患者。
萨哈S、杜塔K、纳亚克PP,《甜蜜的睡眠:史密斯-马吉尼斯综合征中的牙科警示信号》。《国际临床儿科牙科杂志》2024年;17(10):1189 - 1192。