Wevers R A, Hansen S I, van Hellenberg Hubar J L, Holm J, Høier-Madsen M, Jongen P J
Institute of Neurology, University Hospital of Nijmegen, The Netherlands.
J Neurol Neurosurg Psychiatry. 1994 Feb;57(2):223-6. doi: 10.1136/jnnp.57.2.223.
An adult male patient of Dutch ancestry has a slowly progressive neurological disease characterised by a cerebellar syndrome, distal spinal muscular atrophy, pyramidal tract dysfunction, and perceptive hearing loss. A severe folate deficiency state was found in CSF in combination with a normal serum and red cell folate state. Two unknown abnormal metabolites were present in CSF. The concentration of immunoreactive folate binding protein in CSF was unusually low, whereas the concentration of the protein measured with radioligand (3H-folate) binding was unusually high. The transfer of folate over the choroid plexus seems to be disturbed, potentially reflecting a defect in the choroid plexus folate binder.
一名具有荷兰血统的成年男性患者患有一种缓慢进展的神经疾病,其特征为小脑综合征、远端脊髓性肌萎缩、锥体束功能障碍和感音神经性听力损失。脑脊液中发现严重的叶酸缺乏状态,而血清和红细胞叶酸状态正常。脑脊液中存在两种未知的异常代谢物。脑脊液中免疫反应性叶酸结合蛋白的浓度异常低,而用放射性配体(3H-叶酸)结合法测得的该蛋白浓度异常高。叶酸通过脉络丛的转运似乎受到干扰,这可能反映了脉络丛叶酸结合剂的缺陷。