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Evaluation of the ChKd With Developmental Impairments

机译:对发展障碍的CHKD评估

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PURPOSE OF REVIEW: This article discusses the diagnostic evaluation of intellectual developmental disorder, comprising global developmental delay and intellectual disability in children.RECENT FINDINGS: With a prevalence of 1% to 3% and substantial comorbidity, high lifetime costs, and emotional burden, intellectual developmental disorder is characterized by limitations in both intellectual functioning (IQ less than 70) and adaptive behavior starting before 18 years of age. Pinpointing the precise genetic cause is important, as it allows for accurate genetic counseling, avoidance of unnecessary testing, prognostication, and tailored management, which, for an increasing number of genetic conditions, targets the pathophysiology and improves outcomes.SUMMARY: The etiology of intellectual developmental disorder is heterogeneous, which mandates a structured approach that considers family situation, test costs, yield, and potential therapeutic tractability of the identified condition. Diagnosis of an underlying genetic cause is increasingly important with the advent of new treatments. Still, in many cases, the cause remains unknown, and research is needed to elucidate its complex molecular basis.
机译:审查目的:本文讨论了智力发病障碍的诊断评估,包括儿童的全球发育延迟和智力残疾。特点:患病率为1%至3%,高度的合并症,高寿命,知识分子发育障碍的特点是智力运作(IQ少于70)和18岁之前的自适应行为的局限性。精确定位精确的遗传原因是重要的,因为它允许准确的遗传咨询,避免不必要的测试,预测和量身定制的管理,这对于越来越多的遗传条件,旨在使病理生理学和改善结果。估计:知识分子的病因发育障碍是异质的,其授权了一种结构化方法,其考虑了鉴定条件的家庭情况,试验成本,产量和潜在治疗途径。诊断潜在的遗传原因随着新治疗的出现越来越重要。仍然,在许多情况下,原因仍然是未知的,并且需要研究来阐明其复杂的分子基础。

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