Waldman Amy T
Continuum (Minneap Minn). 2018 Feb;24(1, Child Neurology):130-149. doi: 10.1212/CON.0000000000000560.
The leukodystrophies, typically considered incurable neurodegenerative disorders, are often diagnosed after irreversible central and peripheral nervous system injury has occurred. Early recognition of these disorders is imperative to enable potential therapeutic interventions. This article provides a summary of the symptoms of and diagnostic evaluation for leukodystrophies, along with the currently available therapies and recent advances in management.
The leukodystrophies are a rapidly expanding field because of advances in neuroimaging and genetics; however, recognition of the clinical and biochemical features of a leukodystrophy is essential to accurately interpret an abnormal MRI or genetic result. Moreover, the initial symptoms of leukodystrophies may mimic other common pediatric disorders, leading to a delay in the recognition of a degenerative disorder.
This article will aid the clinician in recognizing the clinical features of leukodystrophies and providing accurate diagnosis and management.
脑白质营养不良通常被认为是无法治愈的神经退行性疾病,常在中枢和周围神经系统发生不可逆损伤后才得以诊断。尽早识别这些疾病对于实施潜在的治疗干预至关重要。本文总结了脑白质营养不良的症状和诊断评估方法,以及目前可用的治疗方法和管理方面的最新进展。
由于神经影像学和遗传学的进展,脑白质营养不良领域正在迅速扩展;然而,认识脑白质营养不良的临床和生化特征对于准确解读异常的MRI或基因检测结果至关重要。此外,脑白质营养不良的初始症状可能与其他常见儿科疾病相似,导致对退行性疾病的识别延迟。
本文将帮助临床医生识别脑白质营养不良的临床特征,并提供准确的诊断和管理。