论文部分内容阅读
由单基因突变或缺陷导致物质代谢障碍引起的先天性代谢病常表现为酶缺乏症,为探索某些代谢积蓄病的孕早期产前诊断,作者参照了近年来有关这方面的研究资料,以妊娠6.5——10周经人工流产后完全发育的叶状绒毛为材材,用等电聚集和淀粉凝胶电泳方法,对绒毛的磷酸葡萄糖变位酶,6—磷酸葡萄糖酸脱氢酶,腺苷酸激酶,酸性磷酸酶,酯酶D和腺苷脱氨酶进行了定性分析,共测试187个样品,列出了这六种酶的平均
Congenital metabolic diseases caused by single gene mutations or defects caused by metabolism disorders often show enzyme deficiency, in order to explore some of the metabolic accumulation disease in the first trimester of prenatal diagnosis, the author with reference to recent years in this regard research data to Pregnancy 6.5 - 10 weeks after the full development of human hair follicles after abortion as material, using isoelectric focusing and starch gel electrophoresis method, on the hair of phosphoglucomutase, 6-phosphogluconate dehydrogenase, gland Kinase, acid phosphatase, esterase D and adenosine deaminase were qualitatively analyzed, a total of 187 samples were tested and the average of these six enzymes was listed