Wang Sheng-Jun, Yan Chuan-Zhu, Wen Bing, Zhao Yu-Ying
Department of Neurology, Qilu Hospital, Shandong University, Jinan, China,
Neuropsychiatr Dis Treat. 2019 Feb 21;15:549-555. doi: 10.2147/NDT.S196924. eCollection 2019.
The Cobalamin C (cblC) disease is an inborn error of cobalamin metabolism. Late-onset cblC disease was diagnosed in patients having overt symptoms after 4 years of age. The late-onset cblC disease patients were rare and easily misdiagnosed. This study analyzed the clinical presentations, gene mutations, and treatments of Chinese patients with late-onset cblC disease.
The clinical data of 26 Han Chinese patients diagnosed with late-onset cblC disease were retrospectively analyzed. All patients underwent serum homocysteine level exam, urine concentrations of organic acids measurement, neuroimaging scans, gene analysis, and treatments evaluations.
The mean age at disease onset and diagnosis was 17.8±7.0 years. The most frequent neuropsychiatric disturbances were lower limb weakness (50%), psychiatric disturbances (46.2%), and gait instability (42.3%). The mean methylmalonic acid level in urine was 107.4±56.6 μmol/L, and mean serum total homocysteine was 105.4±41.0 μmol/L. The most common abnormal radioimaging changes were observed in the spinal cord (88%) and brain (32%). Scoliosis was detected in 85.7% of patients. The methylmalonic aciduria and homocystinuria type C protein gene analysis showed that c.482G>A (57.7%) and c.609G>A (34.6%) mutations were the most frequent genotypes. After treatments with hydroxycobalamin, betaine, folic acid, L-carnitine, and compound vitamin B, the clinical features and biochemical parameters of patients with late-onset cblC disease were found to be alleviated.
In our late-onset cblC disease cases, lower limb weakness, psychiatric disturbances, and gait instability were the most frequent manifestations. Patients responded well to the drug treatments with hydrocobalamin and betaine. When juvenile or adult patients with hyperhomocysteinemia present with neurological symptoms, cblC disease needs to be considered.
钴胺素C(cblC)病是一种钴胺素代谢的先天性疾病。迟发性cblC病在4岁以后出现明显症状的患者中被诊断出来。迟发性cblC病患者较为罕见且容易误诊。本研究分析了中国迟发性cblC病患者的临床表现、基因突变及治疗情况。
回顾性分析26例被诊断为迟发性cblC病的汉族患者的临床资料。所有患者均接受了血清同型半胱氨酸水平检测、尿有机酸浓度测定、神经影像学扫描、基因分析及治疗评估。
发病及诊断时的平均年龄为17.8±7.0岁。最常见的神经精神障碍为下肢无力(50%)、精神障碍(46.2%)和步态不稳(42.3%)。尿中甲基丙二酸的平均水平为107.4±56.6μmol/L,血清总同型半胱氨酸的平均水平为105.4±41.0μmol/L。最常见的异常影像学改变见于脊髓(88%)和脑(32%)。85.7%的患者检测出脊柱侧弯。甲基丙二酸尿症和同型胱氨酸尿症C型蛋白基因分析显示,c.482G>A(57.7%)和c.609G>A(34.6%)突变是最常见的基因型。经羟钴胺、甜菜碱、叶酸、左旋肉碱和复合维生素B治疗后,迟发性cblC病患者的临床特征和生化参数得到缓解。
在我们的迟发性cblC病病例中,下肢无力、精神障碍和步态不稳是最常见的表现。患者对羟钴胺和甜菜碱的药物治疗反应良好。当青少年或成年高同型半胱氨酸血症患者出现神经症状时,需考虑cblC病。