Kayser Michael A
Warren Clinic Center for Genetics, Center for Genetic Testing at Saint Francis, 6465 South Yale Avenue, Tulsa, OK 74136, USA.
Semin Pediatr Neurol. 2008 Sep;15(3):127-31. doi: 10.1016/j.spen.2008.05.006.
In the past few years, there has been a veritable explosion in the discovery of "new" inborn errors of metabolism. These new conditions are involved in complex pathways of intermediary metabolism affecting processes heretofore unknown. The phenotypes of these new conditions are in many ways milder than the classically described metabolic disorders. Several of these conditions present as nonsyndromic neurodevelopmental and/or neurobehavioral disorders. As such, these conditions should be considered in the differential diagnosis of conditions such as mental retardation, autism spectrum disorders, movement disorders, and cerebral palsy. This article reviews several of these recently described conditions including the clinical presentation, the biochemical profile, the diagnostic approach, and therapeutic options.
在过去几年里,“新的”先天性代谢缺陷的发现出现了名副其实的激增。这些新情况涉及中间代谢的复杂途径,影响着迄今为止未知的过程。这些新情况的表型在许多方面比经典描述的代谢紊乱更为轻微。其中一些情况表现为非综合征性神经发育和/或神经行为障碍。因此,在对智力发育迟缓、自闭症谱系障碍、运动障碍和脑瘫等疾病进行鉴别诊断时,应考虑这些情况。本文综述了几种最近描述的情况,包括临床表现、生化特征、诊断方法和治疗选择。