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先天性代谢缺陷与癫痫:当前的认识、诊断及治疗方法

Inborn Errors of Metabolism and Epilepsy: Current Understanding, Diagnosis, and Treatment Approaches.

作者信息

Sharma Suvasini, Prasad Asuri N

机构信息

Department of Pediatrics, Lady Hardinge Medical College, New Delhi 110001, India.

Department of Pediatrics and Clinical Neurological Sciences, Schulich School of Medicine and Dentistry, Children's Hospital of Western Ontario and London Health Sciences Centre, London, ON N6A5W9, Canada.

出版信息

Int J Mol Sci. 2017 Jul 2;18(7):1384. doi: 10.3390/ijms18071384.

Abstract

Inborn errors of metabolism (IEM) are a rare cause of epilepsy, but seizures and epilepsy are frequently encountered in patients with IEM. Since these disorders are related to inherited enzyme deficiencies with resulting effects on metabolic/biochemical pathways, the term "metabolic epilepsy" can be used to include these conditions. These epilepsies can present across the life span, and share features of refractoriness to anti-epileptic drugs, and are often associated with co-morbid developmental delay/regression, intellectual, and behavioral impairments. Some of these disorders are amenable to specific treatment interventions; hence timely and appropriate diagnosis is critical to improve outcomes. In this review, we discuss those disorders in which epilepsy is a dominant feature and present an approach to the clinical recognition, diagnosis, and management of these disorders, with a greater focus on primarily treatable conditions. Finally, we propose a tiered approach that will permit a clinician to systematically investigate, identify, and treat these rare disorders.

摘要

先天性代谢缺陷(IEM)是癫痫的罕见病因,但在IEM患者中癫痫发作和癫痫却很常见。由于这些疾病与遗传性酶缺乏有关,进而影响代谢/生化途径,“代谢性癫痫”这一术语可用于涵盖这些病症。这些癫痫可在整个生命周期出现,具有对抗癫痫药物难治的特点,且常伴有共病性发育迟缓/倒退、智力和行为障碍。其中一些疾病可采用特定的治疗干预措施;因此,及时、恰当的诊断对于改善预后至关重要。在本综述中,我们讨论了以癫痫为主要特征的那些疾病,并提出了一种对这些疾病进行临床识别、诊断和管理的方法,更侧重于主要可治疗的病症。最后,我们提出一种分层方法,使临床医生能够系统地调查、识别和治疗这些罕见疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d69f/5535877/2796be72a8e8/ijms-18-01384-g001.jpg

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