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Autism Spectrum Disorder in North-Western Nigeria

机译:尼日利亚西北部的自闭症谱系障碍

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Aim: To determine the profile of autism spectrum disorder (ASD) cases in a tertiary hospital in Sokoto, over a decade. Study Design: A descriptive study on the clinical presentations and associated co-morbidities in children with ASD as seen in Usmanu Danfodiyo University Teaching Hospital (UDUTH) Sokoto. Place and Duration of Study: Department of Paediatrics (Neurology Unit), UDUTH Sokoto, Nigeria, between July 2008 and June, 2018. Methodology: Children with documented features of ASD (as described in DSM-5) over the study period were enrolled. Relevant information was extracted from the hospital records. The DSM 5 diagnostic criteria for ASD was applied, and all cases whose clinical records conform to the DSM 5 criteria, and having complete clinical records were included. Patients with incomplete data were excluded. Co-morbid conditions were identified based on history and examination records. A descriptive analysis of the data was done and presented as frequencies and proportions. Results: Out of the 1267 cases seen in Paediatric Neurology clinic over the study period, 18 cases exhibited the symptoms of ASD based on the DSM 5 criteria, giving a hospital prevalence of 1.4%. The mean age at diagnosis was 5.6 ±2.5 (range 2 to 13) years, with a M:F of 1:1.6. All the cases had the core symptoms of impaired social communication, impaired social interactions and restricted/stereotypic behaviours that started before 3 years of age. Majority (55.6%) of the cases were diagnosed after the age of 5 years. Identified co-morbidities include hyperactivity (55.6%), seizures (33.3%) and motor delays (27.8%), occurring alone or in combinations. Only 4 (22.2%) of the cases had no identifiable neuro-developmental co-morbidities. Conclusion: Autism spectrum Disorder is one of the neurodevelopmental disorders among children with Neurologic problems in our centre and is commonly associated with other co-morbidities. There is need to create more awareness about ASD so as to enhance its early recognition and appropriate interventions.
机译:目的:确定索科托市一家三级医院十多年来自闭症谱系障碍(ASD)病例的概况。研究设计:对描述性研究的一项临床研究及其相关并发症,如乌斯曼努·丹佛迪约大学教学医院(UDUTH)索科托所见。研究的地点和时间:2008年7月至2018年6月,尼日利亚UDUTH索科托儿科(神经科)。方法:研究期间具有ASD特征的儿童(如DSM-5中所述)。从医院记录中提取相关信息。应用针对ASD的DSM 5诊断标准,并包括所有临床记录符合DSM 5标准并具有完整临床记录的病例。数据不完整的患者被排除在外。根据病史和检查记录确定并存病。对数据进行了描述性分析,并以频率和比例表示。结果:在研究期间,小儿神经病学诊所所见的1267例病例中,有18例表现出基于DSM 5标准的ASD症状,医院患病率为1.4%。诊断时的平均年龄为5.6±2.5岁(范围2至13),M:F为1:1.6。所有病例的核心症状都是三岁之前开始的社交沟通受损,社交互动受损和受限/陈规定型行为。大多数病例(55.6%)在5岁以后被诊断出。识别出的合并症包括多动(55.6%),癫痫发作(33.3%)和运动迟缓(27.8%),它们单独或组合出现。只有4例(22.2%)没有可识别的神经发育合并症。结论:自闭症谱系障碍是我们中心神经系统疾病儿童的神经发育障碍之一,通常与其他合并症相关。有必要提高对ASD的认识,以增强对ASD的早期认识和适当的干预措施。

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