识别诱发新生儿癫痫的代谢性疾病。

Pub Date : 2024-05-01 DOI:10.1891/NN-2023-0048
Rebecca L Judy, Joanna L Reynolds, Amy J Jnah
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引用次数: 0

摘要

先天性代谢异常(IEMs)虽然是新生儿癫痫发作的罕见病因,但仍然是控制不佳的新生儿癫痫综合鉴别诊断的重要组成部分。对临床医生来说,诊断新生儿代谢性疾病是一项艰巨的任务;不过,现在各州的常规新生儿筛查项目已包括许多 IEMs。其中有三种疾病--吡哆醇依赖性癫痫、枫糖浆尿病和泽尔维格谱系障碍--与新生儿癫痫和神经认知损伤高度相关,但却经常被误诊。随着围绕这些疾病生物标志物的研究不断涌现,基因测序技术也在不断进步,临床医生开始更好地制定这些疾病的早期识别策略。在这篇文献综述中,作者旨在为临床医生提供一份创新的临床指南,重点介绍与新生儿发作相关的 IEMs,目的是促进优质护理和安全。
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Identifying Metabolic Diseases That Precipitate Neonatal Seizures.

Although a rare cause of neonatal seizures, inborn errors of metabolism (IEMs) remain an essential component of a comprehensive differential diagnosis for poorly controlled neonatal epilepsy. Diagnosing neonatal-onset metabolic conditions proves a difficult task for clinicians; however, routine state newborn screening panels now include many IEMs. Three in particular-pyridoxine-dependent epilepsy, maple syrup urine disease, and Zellweger spectrum disorders-are highly associated with neonatal epilepsy and neurocognitive injury yet are often misdiagnosed. As research surrounding biomarkers for these conditions is emerging and gene sequencing technologies are advancing, clinicians are beginning to better establish early identification strategies for these diseases. In this literature review, the authors aim to present clinicians with an innovative clinical guide highlighting IEMs associated with neonatal-onset seizures, with the goal of promoting quality care and safety.

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