Kesler Shelli R, Schwartz Charles, Stevenson Roger E, Reiss Allan L
Center for Interdisciplinary Brain Sciences Research, Stanford University School of Medicine, 401 Quarry Road, MC5795, Stanford, CA 94305-5795, USA.
Neurogenetics. 2009 Oct;10(4):299-305. doi: 10.1007/s10048-009-0184-2. Epub 2009 Mar 7.
Snyder-Robinson syndrome (SRS) is a form of X-linked mental retardation resulting from mutations in spermine synthase (SMS), which impact neurodevelopment and cognitive outcome. We obtained cerebral, cerebellum, hippocampus, and red nucleus volumes from two males with SRS and 24 age- and gender-matched typically developing controls using volumetric neuroimaging analyses. Total brain volume was enlarged in males with SRS while cerebellum, hippocampus, and red nucleus volumes tended to be reduced compared to controls. Mutations of the X chromosome may modulate the risk for mental retardation through altered early neurodevelopment, disruption in receptor function, and ongoing neural organization and plasticity. Disruption of SMS function may negatively affect regional brain volumes that subserve cognitive and motor abilities. This research provides valuable insight into the effects of polyamine function on brain development.
斯奈德-罗宾逊综合征(SRS)是一种X连锁智力障碍,由精胺合酶(SMS)突变引起,这些突变会影响神经发育和认知结果。我们通过容积神经影像学分析,从两名患有SRS的男性以及24名年龄和性别匹配的正常发育对照者中获取了大脑、小脑、海马体和红核的体积。与对照组相比,患有SRS的男性全脑体积增大,而小脑、海马体和红核体积则有减小的趋势。X染色体的突变可能通过改变早期神经发育、破坏受体功能以及持续的神经组织和可塑性来调节智力障碍的风险。SMS功能的破坏可能会对支持认知和运动能力的区域脑体积产生负面影响。这项研究为多胺功能对大脑发育的影响提供了有价值的见解。