Suppr超能文献

钼辅因子缺乏症:一种易被漏诊的先天性代谢紊乱疾病。

Molybdenum co-factor deficiency: an easily missed inborn error of metabolism.

作者信息

Aukett A, Bennett M J, Hosking G P

机构信息

Dudley Road Hospital, Birmingham.

出版信息

Dev Med Child Neurol. 1988 Aug;30(4):531-5. doi: 10.1111/j.1469-8749.1988.tb04781.x.

Abstract

A female patient is described with combined deficiency of sulphite, zanthine and aldehyde oxidase. She presented at the age of four weeks with intractable seizures. Initially the diagnosis was suspected because of a very low serum urate level (23 mumol/1-1). This condition can be easily missed and it is proposed that measurement of serum urate be included in the metabolic assessment of neonates with unexplained seizures and developmental delay.

摘要

一名患有亚硫酸盐、黄嘌呤和醛氧化酶联合缺乏症的女性患者被报道。她在四周大时出现难治性癫痫发作。最初,由于血清尿酸水平极低(23微摩尔/升)而怀疑有此诊断。这种情况很容易被漏诊,建议将血清尿酸测定纳入对原因不明的癫痫发作和发育迟缓新生儿的代谢评估中。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验