Neuropsychiatric Aspects of Congenital and Genetic Disorders

Sujita Kumar Kar, Jamshed Ahmad, TV Ram Kumar
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Abstract

Neuropsychiatry is an area of medicine that deals with behavioural issues caused by brain dysfunction. It is found at the intersection of neurology and psychiatry. Individuals with congenital and genetic diseases are more likely to experience neuropsychiatric symptoms (particularly mental retardation), which can lead to considerable disability and a lower quality of life. Developmental delay, intellectual disability, autism spectrum disorders (ASDs), and cognitive dysfunction are the most common symptoms of neuropsychiatric illnesses. Many intellectual developmental abnormalities are caused by complex genetic components (such as attention deficit hyperactivity disorder), pregnancy or birth complications, or environmental variables, among other things. Patients with congenital and genetic diseases with neuropsychiatric indications benefit from a multidisciplinary approach to management. Interdepartmental liaisoning may be advantageous in the absence of a multidisciplinary team.
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先天性和遗传性疾病的神经精神方面
神经精神病学是处理由脑功能障碍引起的行为问题的医学领域。它是在神经病学和精神病学的交汇处发现的。患有先天性和遗传性疾病的人更有可能出现神经精神症状(特别是智力迟钝),这可能导致严重的残疾和较低的生活质量。发育迟缓、智力残疾、自闭症谱系障碍(ASDs)和认知功能障碍是神经精神疾病最常见的症状。许多智力发育异常是由复杂的遗传因素(如注意缺陷多动障碍)、妊娠或分娩并发症、或环境变量等因素引起的。具有神经精神指征的先天性和遗传性疾病患者受益于多学科方法的管理。在没有多学科团队的情况下,部门间的联络可能是有利的。
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