Pattern of malocclusion in children living with sickle cell anemia

Q4 Medicine Sahel Medical Journal Pub Date : 2019-10-01 DOI:10.4103/smj.smj_49_18
Orighoye Temisanren, B. Fakuade, F. Ajibade, S. Yuguda, A. Girei
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引用次数: 2

Abstract

Background: Sickle cell anemia is a hereditary disorder of the hematological system. It involves the production of abnormal hemoglobin, which is sickle in shape and has a short life span, resulting in secondary hemopoietic function by the long bones and the jaw bones. The disorder burden not only presents with systemic affectations and morbidity that is commonly observed but also has immense effects on the jaw bones presenting as malocclusion and in severe cases causing gnathopathy and psychosocial disturbance, especially with esthetics. Other dental effects include functional disturbances and diseases of the oral tissue. Objective: The aim of this study is to determine the occlusal pattern of children with sickle cell anemia. Materials and Methods: Consecutive patients attending the Sickle Cell Clinic of the department of Hematology, Federal Teaching Hospital Gombe, aged 6 to 16years. The inclusion criteria included individuals who have been diagnosed to have HbSS using electrophoresis. Sociodemographic data and oral examination were carried out, and dental and occlusal parameters were recorded in a data collection form. Data were analyzed using the SPSS software version 19. The level of statistical significance was set at P < 0.05. Results: The mean age was 10.12 ± 3.10 years. Ninety (55.6%) patients were male. The samples were grouped into two: Group I ages 6–10 years comprising 92 children and ages 11–16 years comprising 70 children in Group II. Angle's Class I molar relationship was observed to be 86 (93.5%) and 57 (81.4%), respectively, for Groups I and II. Overjet and overbite were found to be increased in 34 (37.0%) and 5 (5.4%) for Group I and 23 (32.9%) and 5 (7.1%) for Group II, respectively. Conclusion: The burden of sickle cell anemia is not limited to systemic manifestations alone. Dental presentations that could affect psychosocial, function, health of oral tissues, and speech have also been observed. Therefore, it is expedient that these individuals on presentation to the clinic are examined in a holistic manner with a view to attending to all their presenting problems at an early stage.
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镰状细胞性贫血儿童畸形畸形的模式
背景:镰状细胞性贫血是一种血液系统的遗传性疾病。它涉及到异常血红蛋白的产生,这种血红蛋白呈镰状,寿命短,导致长骨和颌骨的次要造血功能。这种疾病负担不仅表现为常见的全身性影响和发病率,而且对颌骨也有巨大的影响,表现为错颌,在严重的情况下会引起颌病和社会心理障碍,特别是美学障碍。其他对牙齿的影响包括功能紊乱和口腔组织疾病。目的:研究镰状细胞性贫血患儿的咬合模式。材料和方法:连续在贡贝联邦教学医院血液科镰状细胞门诊就诊的患者,年龄6 - 16岁。纳入标准包括经电泳诊断为HbSS的个体。进行了社会人口统计资料和口腔检查,并将牙齿和咬合参数记录在数据收集表中。数据采用SPSS 19版软件进行分析。P < 0.05为差异有统计学意义的水平。结果:平均年龄10.12±3.10岁。男性90例(55.6%)。样本分为两组:第一组6-10岁,包括92名儿童;第二组11-16岁,包括70名儿童。I族和II族的I类摩尔关系分别为86(93.5%)和57(81.4%)。ⅰ组有34例(37.0%)、5例(5.4%)、ⅱ组有23例(32.9%)、5例(7.1%)出现过喷和复咬。结论:镰状细胞性贫血的负担不仅限于全身表现。还观察到可能影响心理社会、功能、口腔组织健康和语言的牙科表现。因此,这是权宜之计,这些个人在介绍到诊所在一个整体的方式进行检查,以出席在早期阶段他们所有的表现问题。
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来源期刊
Sahel Medical Journal
Sahel Medical Journal Medicine-Medicine (all)
CiteScore
0.60
自引率
0.00%
发文量
5
审稿时长
47 weeks
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