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脱髓鞘与单碳转移途径的先天性缺陷。

Demyelination and inborn errors of the single carbon transfer pathway.

作者信息

Surtees R

机构信息

Institute of Child Health (UCLMS), London, UK.

出版信息

Eur J Pediatr. 1998 Apr;157 Suppl 2:S118-21. doi: 10.1007/pl00014296.

Abstract

Inborn errors of the single-carbon transfer pathway are rare disorders of folate and cobalamin metabolism. They may be complicated by demyelination resembling subacute combined degeneration of the cord and brain. The study of CSF metabolites in children with serial errors affecting the single-carbon transfer pathway has suggested that S-adenosylmethionine deficiency is a cause of the demyelination. This deficiency is corrected by treatment that causes clinical improvement and remyelination. Some treatments can only have an indirect effect on the brain and this is discussed with other evidence that the liver may produce factors that are necessary for the maintenance of central myelin.

摘要

单碳转移途径的先天性缺陷是叶酸和钴胺素代谢的罕见疾病。它们可能并发类似脊髓和脑亚急性联合变性的脱髓鞘病变。对影响单碳转移途径的连续性缺陷患儿脑脊液代谢物的研究表明,S-腺苷甲硫氨酸缺乏是脱髓鞘的一个原因。这种缺乏可通过导致临床改善和髓鞘再生的治疗得到纠正。一些治疗只能对大脑产生间接影响,本文将对此进行讨论,同时还将讨论其他证据,即肝脏可能产生维持中枢髓鞘所需的因子。

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