Green A, Hall S M
Department of Clinical Chemistry, Children's Hospital, Birmingham.
Arch Dis Child. 1992 Oct;67(10):1313-7. doi: 10.1136/adc.67.10.1313.
Ten per cent of patients initially reported with Reye's syndrome in the British Isles (1981-91) were subsequently found to have an underlying inherited metabolic disorder (IMD). There was also evidence to suggest that other cases may not have been recognised. The range of metabolic disorders that mimic Reye's syndrome is wide and specialist, often complex, investigations are required to make a specific diagnosis. Those patients presenting with Reye's syndrome-like illness but also with one or more clinical features suggestive of an IMD require particular attention and detailed investigation. Recommendations for specimen collection and investigation are presented.
在不列颠群岛(1981 - 1991年)最初报告患有瑞氏综合征的患者中,10%随后被发现患有潜在的遗传性代谢紊乱(IMD)。也有证据表明其他病例可能未被识别。模仿瑞氏综合征的代谢紊乱范围很广,需要专业的、通常很复杂的检查才能做出明确诊断。那些表现出类似瑞氏综合征疾病但同时具有一种或多种提示IMD临床特征的患者需要特别关注和详细检查。本文给出了标本采集和检查的建议。