Clinical and Laboratory Markers of Hereditary Metabolic Diseases in Children of the First Half of Life

N. N. Martynovich, N. E. Globenko, S. N. Kuznetsova
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Abstract

A significant contribution to the morbidity and mortality of children is due to hereditary pathology, which is manifested by high mortality. Aim of the research. To study the frequency of occurrence, structure and clinical and laboratory markers of hereditary metabolic diseases in children of the first half of the year with suspicion of this pathology. Materials and methods. A retrospective analysis of case histories (form No. 003/y) and a face-to-face examination of patients directed to blood tests by tandem mass spectrometry, from Surgery Unit No. 2 for Newborns and Premature Babies and from the Unit of Pathology of Newborns, (Ivano-Matryoninskaya City Children’s Clinical Hospital, Irkutsk). Results. In 2019, 21 children with suspected hereditary metabolic diseases were examined using the tandem mass spectrometry method in the above mentioned departments. All of them had at least one of the main clinical criteria for hereditary metabolic diseases: 67 % had hepatomegaly in combination with an increase in the level of liver enzymes, 43 % had a hereditary history and metabolic acidosis, 33 % showed a sudden deterioration after a period of normal development, 24 % had hypoglycemia, and 14 % had an abnormal urine or body odor, in 4.7 % of cases there was an increase in ketone bodies in the blood and (or) urine. All children identified from 3 to 7 additional criteria, which are indications for examination on the hereditary metabolic diseases. The results of the study revealed 5 children with hereditary metabolic diseases namely amino acid metabolism. 90 % of them had a burdened hereditary history, 100 % had a concomitant pathology – hepatitis and cholestatic lesions of the liver, anemia, an open oval window and others. Conclusion. Despite the obvious economic and medical significance of preclinical identification of patients with hereditary metabolic diseases, the screening problem contains many open questions that need to be addressed at all levels of the organization.
前半生儿童遗传性代谢性疾病的临床和实验室标志物
造成儿童发病率和死亡率的一个重要原因是遗传病理,这表现为高死亡率。研究的目的。研究上半年疑似遗传性代谢性疾病患儿的发病频率、结构及临床、实验室标志物。材料和方法。回顾性分析病历(003/y号表格),并对新生儿和早产儿第二外科病房和新生儿病理病房(伊尔库茨克伊万诺- matryoninskaya市儿童临床医院)的患者进行面对面检查,通过串联质谱法进行血液检查。结果。2019年对上述科室21例疑似遗传性代谢性疾病患儿进行串联质谱检测。他们所有人都至少有一个主要的遗传性代谢疾病临床标准:67%有肝肿大结合肝酶水平的增加,43%有历史遗传和代谢性酸中毒,33%显示突然恶化经过一段时间的正常发展,低血糖,24%和14%有异常尿液或体味,在4.7%的病例有增加血液中酮体和(或)尿液。所有儿童确定了3至7项额外标准,这些标准是遗传代谢疾病检查的指征。研究结果显示5名儿童患有遗传性代谢性疾病,即氨基酸代谢。其中90%的人有沉重的遗传史,100%的人有伴随的病理-肝炎和肝脏的胆汁淤积性病变,贫血,一个开放的椭圆窗等。结论。尽管对遗传性代谢性疾病患者的临床前鉴定具有明显的经济和医学意义,但筛查问题包含许多悬而未决的问题,需要在组织的各个层面加以解决。
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