Abstract
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.
Cite
CITATION STYLE
Rilstone, J. J., Alkhater, R. A., & Minassian, B. A. (2013). Brain Dopamine–Serotonin Vesicular Transport Disease and Its Treatment. New England Journal of Medicine, 368(6), 543–550. https://doi.org/10.1056/nejmoa1207281
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.