Suppr超能文献

费萨尔国王专科医院及研究中心对沙特有机酸代谢紊乱的治疗经验。

Experience of King Faisal Specialist Hospital and Research Center with Saudi organic acid disorders.

作者信息

Rashed M, Ozand P T, al Aqeel A, Gascon G G

机构信息

Department of Pediatrics, King Faisal Specialist Hospital, Riyadh, Saudi Arabia.

出版信息

Brain Dev. 1994 Nov;16 Suppl:1-6. doi: 10.1016/0387-7604(94)90090-6.

Abstract

The Inborn Errors of Metabolism and Neurology Services of the King Faisal Specialist Hospital and Research Centre (KFSH&RC) and Armed Forces Hospital have received more than 1,500 patients suspected of having an organic acid disorder (OAD) during a period of four years. Of these, 307 patients suspected of having an organic acid disorder (OAD) during a period of four years. Of these, 307 patients, approximately 20%, had a clearly identifiable disorder. Identified OAD's constituted one-quarter of all patients diagnosed as having various types of inborn errors of metabolism during this period, in these clinical services. Prolonged follow-up was available in the majority of cases, allowing detailed clinical, neuroradiologic and neurophysiologic descriptions. Fifty patients (16%) had rare disorders by standards in the West. Approximately 25% were 'neurologic organic acidurias.' This is a new term we are introducing for OAD's manifesting primarily with neurologic signs, but without appreciable acidosis, hypoglycemia or hyperammonemia. In this special issue, we present the KFSH&RC experience with the rare disorders as individual articles. We estimate the frequency of OAD's in Saudi Arabia as 1/740 births. The increased frequency of OAD's in Saudi Arabia is probably due to increased consanguinity, since most OAD's occurred in excess in certain tribes; and due to increased surveillance and testing by our group. Saudi Arabia provides a unique opportunity for research in this area of pediatrics.

摘要

费萨尔国王专科医院及研究中心(KFSH&RC)和武装部队医院的先天性代谢缺陷与神经科服务部门在四年时间里接待了1500多名疑似患有有机酸血症(OAD)的患者。其中,在四年时间里有307名疑似患有有机酸血症(OAD)的患者。在这些患者中,约20%(307名患者)患有明确可辨的疾病。在此期间,在这些临床服务中,确诊的有机酸血症占所有被诊断患有各种类型先天性代谢缺陷患者的四分之一。大多数病例都有长期随访,从而能够进行详细的临床、神经放射学和神经生理学描述。按照西方标准,50名患者(16%)患有罕见疾病。约25%为“神经性有机酸尿症”。这是我们新提出的一个术语,用于描述主要表现为神经体征,但无明显酸中毒、低血糖或高氨血症的有机酸血症。在本期特刊中,我们将KFSH&RC对罕见疾病的经验作为单独文章呈现。我们估计沙特阿拉伯有机酸血症的发病率为1/740活产。沙特阿拉伯有机酸血症发病率的增加可能是由于近亲结婚增加,因为大多数有机酸血症在某些部落中高发;也由于我们团队加强了监测和检测。沙特阿拉伯为该儿科领域的研究提供了独特的机会。

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