神经影像学
先天性代谢错误
医学
高氨血症
儿科
异染性白质营养不良
氨基酸代谢
新生儿筛查
神经科学
疾病
生物信息学
作者
Carlos Ferreira,Clara D.M. van Karnebeek
出处
期刊:Handbook of Clinical Neurology
日期:2019-01-01
卷期号:: 449-481
被引量:24
标识
DOI:10.1016/b978-0-444-64029-1.00022-9
摘要
Inborn errors of metabolism, also known as inherited metabolic diseases, constitute an important group of conditions presenting with neurologic signs in newborns. They are individually rare but collectively common. Many are treatable through restoration of homeostasis of a disrupted metabolic pathway. Given their frequency and potential for treatment, the clinician should be aware of this group of conditions and learn to identify the typical manifestations of the different inborn errors of metabolism. In this review, we summarize the clinical, laboratory, electrophysiologic, and neuroimaging findings of the different inborn errors of metabolism that can present with florid neurologic signs and symptoms in the neonatal period.
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