Pulp Treatment Management of Primary Molars in Patient with Fanconi Anemia: A Case Report

N. Nourbakhsh, Mona Esmaeli
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Abstract

Introduction: Fanconi anemia is a rare autosomal recessive disease that is associated with chromosome failure and impaired DNA repair. The aim of this study was to report a case of Fanconi anemia and to manage the treatment of deciduous tooth pulp and its periodic clinical follow-up. Case Report: The patient is a six-year-old boy with a definitive diagnosis of Fanconi anemia who referred to the Pediatric Dentistry Department of Isfahan University of Medical Sciences with a complaint of deciduous tooth decay and pain on chewing food. The patient had prominent signs like short stature, hirsutism, pigmented face, contiguous eyebrows, coarse hair, protruding forehead, flat nose bridge and large ears. Conclusion: Despite the low platelet count, it was possible to treat two teeth simultaneously in one session and no particular problem has been observed until the case is reported. It is recommended that taking into account the general health of the patient is very important in providing a treatment plan.
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范可尼贫血患者原发磨牙牙髓治疗1例
范可尼贫血是一种罕见的常染色体隐性遗传病,与染色体失效和DNA修复受损有关。本研究报告1例范可尼贫血,探讨乳牙髓的治疗及定期临床随访。病例报告:患者是一名确诊为范可尼贫血的6岁男孩,因乳牙蛀牙和咀嚼食物疼痛而转诊至伊斯法罕医科大学儿科牙科。患者有身材矮小、多毛、面部色素沉着、眉毛相邻、毛发粗糙、前额突出、鼻梁扁平、耳朵大等显著体征。结论:尽管血小板计数低,但一次治疗两颗牙齿是可能的,在此病例报告之前没有观察到特别的问题。建议在提供治疗计划时考虑到患者的总体健康状况是非常重要的。
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