Institute of Medical Science, University of Toronto, Toronto, ON, Canada.
N Engl J Med. 2013 Feb 7;368(6):543-50. doi: 10.1056/NEJMoa1207281. Epub 2013 Jan 30.
We describe a disease encompassing infantile-onset movement disorder (including severe parkinsonism and nonambulation), mood disturbance, autonomic instability, and developmental delay, and we describe evidence supporting its causation by a mutation in SLC18A2 (which encodes vesicular monoamine transporter 2 [VMAT2]). VMAT2 translocates dopamine and serotonin into synaptic vesicles and is essential for motor control, stable mood, and autonomic function. Treatment with levodopa was associated with worsening, whereas treatment with direct dopamine agonists was followed by immediate ambulation, near-complete correction of the movement disorder, and resumption of development.
我们描述了一种疾病,其特征为婴儿期起病的运动障碍(包括严重的帕金森病和不能行走)、情绪障碍、自主神经不稳定和发育迟缓,我们还描述了支持该疾病由 SLC18A2 基因突变引起的证据(该基因编码囊泡单胺转运体 2 [VMAT2])。VMAT2 将多巴胺和血清素转运到突触小泡中,对运动控制、稳定的情绪和自主功能至关重要。左旋多巴治疗与病情恶化相关,而直接多巴胺激动剂治疗后立即能够行走,运动障碍几乎完全纠正,且发育恢复。