Lee Wang-Tso, Lin Jui-Hsiang, Weng Wen-Chin, Peng Steven Shinn-Forng
Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Clinical Center for Neuroscience and Behavioral Medicines, National Taiwan University Hospital, Taipei, Taiwan.
Hum Brain Mapp. 2017 Mar;38(3):1532-1540. doi: 10.1002/hbm.23470. Epub 2016 Nov 17.
Aromatic L-amino acid decarboxylase (AADC) deficiency is an uncommon inherited neurometabolic disease. The clinical presentations and MR findings in children with AADC deficiency were investigated. Total 12 children (6 boys, 6 girls), aged from 9 to 50 months (mean, 23 ±13 months), with AADC deficiency, were enrolled for analysis. Of 12 patients enrolled, clinical presentations included global developmental delay with generalized hypotonia in 12 (100%), dystonia in 12 (100%), oculogyric crisis in 12 (100%), and excessive sweating in 8 (67%). Sleep problem was also found in 4 (33%). Of 15 MR examinations, the major changes included 6 (40%) with diffusely prominent bilateral frontal sulci, 10 (67%) with prominent frontal horns, and 12 (80%) with hypomyelination. In AADC patients, the frontal horn was significantly widened (P < 0.01), and the volume of caudate nucleus was also significantly smaller than that of controls (P = 0.02). The ratios of thickness of the splenium to that of the genu of corpus callosum were also significantly increased (P < 0.01). There was also significant decrease of fiber density indices in major white matter fiber tracts. Using Tract-Based Spatial Statistics approach, we also revealed significant change in major fiber tracts related to language function and motor function. In conclusion, the present study indicated that AADC deficiency may have significant impact on brain development, especially the frontal lobe and fiber tracts related to language function and motor function. Long-term follow-up of brain MRI in patients with AADC deficiency may clarify the possible effect of AADC deficiency on brain development. Hum Brain Mapp 38:1532-1540, 2017. © 2016 Wiley Periodicals, Inc.
芳香族L-氨基酸脱羧酶(AADC)缺乏症是一种罕见的遗传性神经代谢疾病。对患有AADC缺乏症的儿童的临床表现和磁共振成像(MR)结果进行了研究。共有12名年龄在9至50个月(平均23±13个月)的AADC缺乏症儿童(6名男孩,6名女孩)被纳入分析。在纳入的12例患者中,临床表现包括12例(100%)全面发育迟缓伴全身肌张力减退、12例(100%)肌张力障碍、12例(100%)动眼危象和8例(67%)多汗。4例(33%)还存在睡眠问题。在15次MR检查中,主要变化包括6例(40%)双侧额叶沟弥漫性增宽、10例(67%)额角增宽和12例(80%)髓鞘形成不良。在AADC患者中,额角明显增宽(P<0.01),尾状核体积也明显小于对照组(P=0.02)。胼胝体压部与膝部厚度之比也显著增加(P<0.01)。主要白质纤维束的纤维密度指数也显著降低。使用基于体素的空间统计学方法,我们还发现与语言功能和运动功能相关的主要纤维束有显著变化。总之,本研究表明AADC缺乏症可能对脑发育有显著影响,尤其是额叶以及与语言功能和运动功能相关的纤维束。对AADC缺乏症患者进行脑MRI长期随访可能会阐明AADC缺乏症对脑发育的可能影响。《人类大脑图谱》38:1532 - 1540,2017年。©2016威利期刊公司