Boronat Susana, Mehan William A, Shaaya Elias A, Thibert Ronald L, Caruso Paul
Department of Neurology, Massachusetts General Hospital, Boston, MA, USA Department of Pediatric Neurology, Vall d'Hebron Hospital, Universitat Autònoma de Barcelona, Barcelona, Spain
Department of Neuroradiology, Massachusetts General Hospital, Boston, MA, USA.
J Child Neurol. 2015 Mar;30(3):333-8. doi: 10.1177/0883073814538669. Epub 2014 Jun 30.
Patients with 15q duplication syndromes, including isodicentric chromosome 15 and interstitial duplications, usually present with autism spectrum disorder, intellectual disability, and frequently epilepsy. Neuroimaging studies in these patients are typically reported as normal, but nonspecific findings such as thinning of the corpus callosum and increased pericerebral spaces have been reported. A review of brain magnetic resonance imaging (MRI) studies of 11 individuals seen at the Massachusetts General Hospital Dup15q Center was performed. Hippocampus morphology was specifically reviewed, as a recent neuropathologic study has found frequent hippocampal heterotopias and dysplasias in these disorders. Two subjects had unilateral hippocampal sclerosis and 6 had bilateral hippocampal malformations. Hypoplasia of the corpus callosum was present in 2 subjects.
患有15q重复综合征的患者,包括等臂染色体15和间质性重复,通常表现为自闭症谱系障碍、智力残疾,且经常伴有癫痫。这些患者的神经影像学研究通常报告为正常,但也有报告称存在胼胝体变薄和脑周间隙增宽等非特异性表现。对在麻省总医院Dup15q中心就诊的11名个体的脑磁共振成像(MRI)研究进行了回顾。由于最近的一项神经病理学研究发现这些疾病中经常出现海马体异位和发育异常,因此对海马体形态进行了专门回顾。两名受试者患有单侧海马体硬化,6名受试者患有双侧海马体畸形。两名受试者存在胼胝体发育不全。