Tubbs R Shane, Oakes W Jerry
Department of Cell Biology, University of Alabama at Birmingham, USA.
J Child Neurol. 2003 Jul;18(7):496-8. doi: 10.1177/08830738030180070801.
We report a child with Costello syndrome and Chiari I malformation. The medical literature has several case reports of findings peculiar for each of these two clinical entities that, when investigated, can actually be found in both processes. Recent reports have shown additional medical coincidences for the Chiari I malformation, which, unlike the Chiari II malformation, was once thought not to have many additional associations. We propose that both Costello syndrome and other clinical entities that have potential mesodermal or ectodermal deficiencies (eg, Chiari I malformation and phakomatoses, respectively) could have common dysgeneses. Further case reports from other institutions regarding Costello syndrome and Chiari I malformation are now necessary to confirm our findings. Our hope is that these data will potentially add to our knowledge of the etiology of both Costello syndrome and Chiari I malformation and potentially aid in the definition of a genetic locus for both entities.
我们报告了一名患有科斯特洛综合征和 Chiari I 畸形的儿童。医学文献中有几例关于这两种临床病症各自特殊表现的病例报告,经研究发现,在这两种病症中实际上都能找到这些表现。最近的报告显示 Chiari I 畸形还存在其他医学上的巧合情况,与 Chiari II 畸形不同,Chiari I 畸形曾被认为没有太多其他关联。我们认为,科斯特洛综合征以及其他具有潜在中胚层或外胚层缺陷的临床病症(例如分别为 Chiari I 畸形和 phakomatoses)可能存在共同的发育异常。现在需要其他机构提供更多关于科斯特洛综合征和 Chiari I 畸形的病例报告来证实我们的发现。我们希望这些数据可能会增加我们对科斯特洛综合征和 Chiari I 畸形病因的了解,并有可能有助于确定这两种病症的基因位点。