Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, Ansari Nagar, New Delhi 110029, India.
Indian J Pediatr. 2011 Jul;78(7):854-9. doi: 10.1007/s12098-011-0422-0. Epub 2011 Jun 18.
Diagnosis of inborn errors of metabolism (IEM) such as an organic acidemia or urea cycle defects requires high index of suspicion in a critically ill infant as these conditions mimic common pediatric illnesses. Prompt initiation of the treatment is mandatory even if a definitive diagnosis is not established immediately. Initial screening investigations may give clues and help to classify these disorders in broad categories. It is of utmost importance to preserve samples for testing.
诊断先天性代谢缺陷(IEM),如有机酸血症或尿素循环缺陷,需要对危重症婴儿保持高度怀疑,因为这些病症与常见儿科疾病相似。即使不能立即明确诊断,也必须立即开始治疗。初步筛查检查可能会提供线索,并有助于将这些疾病进行广泛分类。保存样本进行检测至关重要。