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马来西亚通过选择性筛查检测到的先天性代谢缺陷导致的早期死亡

Early Mortalities From Inborn Errors of Metabolism Detected By Selective Screening in Malaysia.

作者信息

Habib Anasufiza, Abdul Malik Nur Aisyah, Abu Yamin Azzah Hana, Abdul Rahman Salina, Apparow Saraswathy, Wan Mahiyuddin Wan Rozita, Yakob Yusnita, Lock Hock Ngu

机构信息

National Institutes of Health, Kuala Lumpur, Malaysia.

Ministry of Health Malaysia, Putrajaya, Malaysia.

出版信息

Sage Open Pediatr. 2025 Apr 2;12:30502225251312056. doi: 10.1177/30502225251312056. eCollection 2025 Jan-Dec.

Abstract

Newborn screening in Malaysia includes congenital hypothyroidism and glucose-6-phosphate dehydrogenase deficiency. Screening for inborn errors of metabolism (IEM) is typically offered only for symptomatic patients. This study aimed to review the clinical and biochemical characteristics of children who experienced early mortality because of IEM. Malaysian children who were diagnosed with IEM and died before 5 years of age, were identified through selective screening of 36 467 at-risk patients between January 2015 and December 2021. Thirty-six cases were detected. The mortality rate of children under 5 years diagnosed with IEM was 1.4 per 10 000 population. Clinical symptoms overlapped across the different IEM groups, and notably, similar organic compounds were found in different types of IEM. The mortality rate due to IEM is significant in Malaysia and most mortalities occurring during the neonatal period.

摘要

马来西亚的新生儿筛查项目包括先天性甲状腺功能减退症和葡萄糖-6-磷酸脱氢酶缺乏症。对于先天性代谢缺陷(IEM),通常仅对有症状的患者进行筛查。本研究旨在回顾因IEM导致早期死亡的儿童的临床和生化特征。通过对2015年1月至2021年12月期间36467名高危患者进行选择性筛查,确定了在马来西亚被诊断为IEM且在5岁前死亡的儿童。共检测到36例。诊断为IEM的5岁以下儿童的死亡率为每10000人中有1.4例。不同IEM组的临床症状存在重叠,值得注意的是,在不同类型的IEM中发现了相似的有机化合物。在马来西亚,IEM导致的死亡率很高,且大多数死亡发生在新生儿期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcc9/12220296/f932db2ea55a/10.1177_30502225251312056-fig1.jpg

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