Suppr超能文献

埃及儿童有机酸尿症:高危筛查的迫切需求。

Organic acidurias in Egyptian children: The urge for high-risk screening.

作者信息

Mehaney Dina A, Seliem Zeinab S, Selim Laila A, Khalil Mona S, Abou-Youssef Hazem S, Elsayed Elham M, Abdou Doaa M, Rizzo Cristiano, Dioniasi-Vici Carlo, Abdelazim Aya M, Elkady Sherihan H

机构信息

Clinical and Chemical Pathology Department, Cairo University, Cairo, Egypt.

Gas Chromatography-Mass Spectrometry laboratory, Cairo University Children Hospital, Cairo, Egypt.

出版信息

Pediatr Int. 2023 Jan;65(1):e15469. doi: 10.1111/ped.15469.

Abstract

BACKGROUND

Organic acidurias are a group of inborn errors of metabolism. They present a significant diagnostic challenge and are associated with serious morbidity and mortality. They are considered the most frequent inborn errors of metabolism among high-risk children. Gas chromatography-mass spectrometry is a reliable diagnostic technique for organic acidurias. This hospital-based study aimed to quantify the frequency of organic acidurias among a group of high-risk Egyptian pediatric patients and to highlight the importance of high-risk screening for such disorders.

METHODS

One hundred and fifty high-risk children who presented to the inherited metabolic disease unit and the pediatric intensive care units of Cairo University Children Hospital were tested for urine organic acids using gas chromatography-mass spectrometry.

RESULTS

Thirty percent (45/150) of the patients were confirmed as having an altered organic acids profile. Neurological manifestations were the most common presentation. Glutaric aciduria type I and maple-syrup urine disease were the most common disorders encountered among the group that was studied.

CONCLUSION

Organic acid detection by gas chromatography-mass spectrometry is key to the diagnosis of many metabolic disorders. Until a national expanded newborn screening program is established, high-risk screening is strongly encouraged for the early detection of, and proper intervention for such disorders among Egyptian children.

摘要

背景

有机酸尿症是一组先天性代谢缺陷病。它们带来了重大的诊断挑战,且与严重的发病率和死亡率相关。它们被认为是高危儿童中最常见的先天性代谢缺陷病。气相色谱-质谱联用技术是诊断有机酸尿症的可靠技术。这项基于医院的研究旨在量化一组高危埃及儿科患者中有机酸尿症的发生率,并强调对此类疾病进行高危筛查的重要性。

方法

对开罗大学儿童医院遗传代谢病科和儿科重症监护病房收治的150名高危儿童进行气相色谱-质谱联用技术检测尿有机酸。

结果

30%(45/150)的患者被确诊有机酸谱异常。神经学表现是最常见的症状。戊二酸尿症I型和枫糖尿症是所研究群体中最常见的疾病。

结论

通过气相色谱-质谱联用技术检测有机酸是诊断许多代谢紊乱疾病的关键。在建立全国范围的扩大新生儿筛查项目之前,强烈建议对埃及儿童进行高危筛查,以便早期发现此类疾病并进行适当干预。

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