Mitnick R J, Bello J A, Shprintzen R J
Department of Radiology, Montefiore Medical Center, Bronx, New York.
Am J Med Genet. 1994 Jun 15;54(2):100-6. doi: 10.1002/ajmg.1320540204.
Magnetic resonance imaging of the brain in 11 consecutively referred patients with velo-cardiofacial syndrome (VCF) showed anomalies in nine cases including small vermis, cysts adjacent to the frontal horns, and small posterior fossa. Focal signal hyperintensities in the white matter on long TR images were also noted. The nine patients showed a variety of behavioral abnormalities including mild developmental delay, learning disabilities, and characteristic personality traits typical of this common multiple anomaly syndrome which has been related to a microdeletion at 22q11. Analysis of the behavioral findings showed no specific pattern related to the brain anomalies, and the patients with VCF who did not have detectable brain lesions also had behavioral abnormalities consistent with VCF. The significance of the lesions is not yet known, but the high prevalence of anomalies in this sample suggests that structural brain abnormalities are probably common in VCF.
对11例连续转诊的腭心面综合征(VCF)患者进行脑部磁共振成像检查,结果显示9例存在异常,包括小脑蚓部小、额叶角旁囊肿和后颅窝小。在长TR图像上还发现白质有局灶性信号增强。这9例患者表现出多种行为异常,包括轻度发育迟缓、学习障碍以及这种常见的多发畸形综合征典型的特征性人格特质,该综合征与22q11微缺失有关。对行为学结果的分析表明,未发现与脑部异常相关的特定模式,且没有可检测到脑部病变的VCF患者也有与VCF相符的行为异常。这些病变的意义尚不清楚,但该样本中异常的高发生率表明,脑部结构异常在VCF中可能很常见。