Comorbidity of cerebral palsy and epilepsy with autism in children

B. A. Abusueva, M. A. Askevova, M. D. Shanavazova, B. M. Nasrutdinova, M. Bobylova, A. S. Gadzhieva
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Abstract

Background. Cerebral palsy is often combined with epilepsy (up to about 50 % of children). The treatment of epilepsy limits the rehabilitation of cerebral palsy, and the rehabilitation of cerebral palsy often provokes epileptic seizures. Epilepsy in children with cerebral palsy is often manifested in a form of developmental and epileptic encephalopathy with spike-and-wave activation in sleep, which is characterized by epileptiform activity according to the type of benign epileptiform patterns of childhood with a high index on the electroencephalogram (up to 100 %), severe epileptic seizures of a status course, and mental disorders by type autism-like behavior (the so-called atypical autism) and disorders of speech communication. The problem of comorbidity of cerebral palsy, epilepsy and autism remains relevant and needs further study.Aim. To study the features of autism spectrum disorder in a group of children with a combination of cerebral palsy and epilepsy.Materials and methods. We examined 100 patients aged 3–10 years with various forms of cerebral palsy, combined with epilepsy, to identify the clinical features of autism spectrum disorder. Criteria for inclusion in the study: age 3–10 years; verified diagnosis of epilepsy in combination with cerebral palsy and autism spectrum disorder; informed consent of the patient’s parents to participate in the study. Criteria for exclusion from the study: severe somatic diseases and disorders of the sense organs (in particular, kyphoscoliosis, gastrostomy and others, as well as deafness, blindness); age less than 3 or more than 10 years.Results. The average age of visiting a psychiatrist was 5.4 ± 0.5 years. The reasons for visit were: violation of the communication (76 %), decreased eye contact (75 %), lack of compassion for surrounding or adjacent animals (100 %), dysphoric disorders (77.1 %), aggression (55 %), autoaggression (40 %), phobias (90 %), impaired speech development (18 %). Perinatal brain damage was diagnosed in 100 % of cases. Epilepsy was manifested by focal motor seizures. Patients with complex treatment (drugs and pedagogical correction) have more pronounced positive dynamics compared with patients who received only drug therapy or only rehabilitation (p <0.05).Conclusion. In children with a combination of cerebral palsy and epilepsy, the cause of autism is perinatal lesions of the central nervous system, as well as the severity of motor pathology and the presence of continued epileptiform activity on the electroencephalogram. Autism in this group of children requires timely recognition and medical and pedagogical correction.
儿童脑瘫和癫痫与自闭症的并发症
背景。脑瘫常与癫痫合并(高达50%的儿童)。癫痫的治疗限制了脑瘫的康复,而脑瘫的康复又常常诱发癫痫发作。脑瘫患儿的癫痫通常表现为发育性和癫痫性脑病,在睡眠中出现尖波激活,其特征是癫痫样活动,根据儿童期良性癫痫样模式的类型,脑电图指数高(高达100%),严重癫痫发作的状态过程,精神障碍的类型是自闭症样行为(所谓的非典型自闭症)和语言交流障碍。脑瘫、癫痫和自闭症的合并症问题仍然存在,需要进一步研究。目的:探讨脑瘫合并癫痫患儿自闭症谱系障碍的特点。材料和方法。我们检查了100例3-10岁的不同形式的脑瘫合并癫痫的患者,以确定自闭症谱系障碍的临床特征。入选标准:年龄3-10岁;癫痫合并脑瘫、自闭症谱系障碍的确诊患者家长知情同意参加本研究。排除在研究之外的标准:严重的躯体疾病和感觉器官紊乱(特别是脊柱后凸、胃造口术和其他疾病,以及耳聋、失明);年龄小于3岁或大于10岁。平均就诊年龄为5.4±0.5岁。访视原因为:违反交流(76%),减少眼神交流(75%),对周围或邻近动物缺乏同情心(100%),烦躁不安(77.1%),攻击(55%),自身攻击(40%),恐惧症(90%),语言发育障碍(18%)。围产期脑损伤的诊断率为100%。癫痫表现为局灶性运动发作。与单纯药物治疗或单纯康复治疗相比,综合治疗(药物+教学矫正)的患者有更显著的积极动力(p <0.05)。在脑瘫和癫痫合并的儿童中,自闭症的原因是围产期中枢神经系统的损伤,以及运动病理的严重程度和脑电图上持续的癫痫样活动的存在。这类儿童的自闭症需要及时识别,并进行医学和教学上的纠正。
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