Roshan Lal Tamanna R, Kliewer Mark A, Lopes Thelma, Rebsamen Susan L, O'Connor Julia, Grados Marco A, Kimball Amy, Clemens Julia, Kline Antonie D
Am J Med Genet C Semin Med Genet. 2016 Jun;172(2):190-7. doi: 10.1002/ajmg.c.31503. Epub 2016 May 10.
Neurobehavioral and developmental issues with a broad range of deficits are prominent features of Cornelia de Lange syndrome (CdLS), a disorder due to disruption of the cohesin protein complex. The etiologic relationship of these clinical findings to anatomic abnormalities on neuro-imaging studies has not, however, been established. Anatomic abnormalities in the brain and central nervous system specific to CdLS have been observed, including changes in the white matter, brainstem, and cerebellum. We hypothesize that location and severity of brain abnormalities correlate with clinical phenotype in CdLS, as seen in other developmental disorders. In this study, we retrospectively evaluated brain MRI studies of 15 individuals with CdLS and compared these findings to behavior at the time of the scan. Behavior was assessed using the Aberrant Behavior Checklist (ABC), a validated behavioral assessment tool with several clinical features. Ten of fifteen (67%) of CdLS patients had abnormal findings on brain MRI, including cerebral atrophy, white matter changes, cerebellar hypoplasia, and enlarged ventricles. Other findings included pituitary tumors or cysts, Chiari I malformation and gliosis. Abnormal behavioral scores in more than one behavioral area were seen in all but one patient. All 5 of the 15 (33%) patients with normal structural MRI studies had abnormal ABC scores. All normal ABC scores were noted in only one patient and this was correlated with moderately abnormal MRI changes. Although our cohort is small, our results suggest that abnormal behaviors can exist in individuals with CdLS in the setting of relatively normal structural brain findings. © 2016 Wiley Periodicals, Inc.
科妮莉亚·德朗格综合征(CdLS)的突出特征是存在广泛缺陷的神经行为和发育问题,这是一种由于黏连蛋白复合体破坏引起的疾病。然而,这些临床发现与神经影像学研究中的解剖学异常之间的病因关系尚未确立。已观察到CdLS特有的大脑和中枢神经系统解剖学异常,包括白质、脑干和小脑的变化。我们假设,正如在其他发育障碍中所见,CdLS患者大脑异常的位置和严重程度与临床表型相关。在本研究中,我们回顾性评估了15例CdLS患者的脑部MRI研究,并将这些发现与扫描时的行为进行了比较。使用异常行为检查表(ABC)评估行为,这是一种具有多种临床特征的经过验证的行为评估工具。15例CdLS患者中有10例(67%)脑部MRI有异常发现,包括脑萎缩、白质变化、小脑发育不全和脑室扩大。其他发现包括垂体肿瘤或囊肿、Chiari I畸形和胶质增生。除1例患者外,所有患者在不止一个行为领域的行为评分均异常。15例(33%)结构MRI研究正常的患者中有5例ABC评分异常。仅1例患者ABC评分正常,且这与中度异常的MRI变化相关。尽管我们的队列规模较小,但我们的结果表明,在大脑结构相对正常的情况下,CdLS患者可能存在异常行为。© 2016威利期刊公司