Saudubray Jean-Marie, Garcia-Cazorla Àngels
Department of Neurology, Neurometabolic Unit, Hopital Pitié Salpétrière, 47-83 Boulevard de l'Hopital, Paris 75013, France.
Neurology Department, Neurometabolic Unit, Hospital Sant Joan de Deu and CIBERER-ISCIII, Passeig Sant Joan de Deu 28950 Esplugues de Llobregat, Barcelona, Spain.
Pediatr Clin North Am. 2018 Apr;65(2):179-208. doi: 10.1016/j.pcl.2017.11.002.
The specialty of inherited metabolic disease is at the forefront of progress in medicine, with new methods in metabolomics and genomics identifying the molecular basis for a growing number of conditions and syndromes. This review presents an updated pathophysiologic classification of inborn errors of metabolism and a method of clinical screening in neonates, late-onset emergencies, neurologic deterioration, and other common clinical scenarios. When and how to investigate a metabolic disorder is presented to encourage physicians to use sophisticated biochemical investigations and not miss a treatable disorder.
遗传性代谢疾病专业处于医学进展的前沿,代谢组学和基因组学的新方法正在确定越来越多病症和综合征的分子基础。本综述介绍了先天性代谢缺陷的最新病理生理分类以及新生儿、迟发性急症、神经功能恶化和其他常见临床情况的临床筛查方法。阐述了何时以及如何对代谢紊乱进行调查,以鼓励医生采用精密的生化检查,避免漏诊可治疗的疾病。