Kim Nam-Sik, Park Sung-Hee
Department of Physical Medicine and Rehabilitation, Chonbuk National University Medical School, Jeonju, Korea.
Ann Rehabil Med. 2017 Aug;41(4):701-704. doi: 10.5535/arm.2017.41.4.701. Epub 2017 Aug 31.
Joubert syndrome (JS) is a rare genetic disorder characterized by a congenital malformation of the hindbrain, and accompanied by axonal decussation abnormalities affecting the corticospinal tract and the superior cerebellar peduncles. To the best of our knowledge, there are no reports of normal pyramidal decussation in JS. Here, we describe the case of an 18-year-old boy presenting midline-crossing corticospinal projections, which were considered normal corticospinal tract trajectories. Diffusion tensor imaging and motor evoked potential study analysis demonstrated the exclusive presence of decussating corticospinal projections in the patient. Based on these results, we suggest that JS might be associated with several, diverse corticospinal motor tract organization patterns.
乔伯特综合征(JS)是一种罕见的遗传性疾病,其特征为后脑先天性畸形,并伴有影响皮质脊髓束和小脑上脚的轴突交叉异常。据我们所知,尚无关于乔伯特综合征中锥体交叉正常的报道。在此,我们描述了一名18岁男孩的病例,该男孩呈现出中线交叉的皮质脊髓投射,被认为是正常的皮质脊髓束轨迹。扩散张量成像和运动诱发电位研究分析表明,该患者仅存在交叉的皮质脊髓投射。基于这些结果,我们认为乔伯特综合征可能与多种不同的皮质脊髓运动束组织模式有关。