Grabowski G A, Kruse J R, Goldberg J D, Chockkalingam K, Gordon R E, Blakemore K J, Mahoney M J, Desnick R J
Am J Hum Genet. 1984 Nov;36(6):1369-78.
The prenatal diagnosis of Tay-Sachs disease was made in two at-risk fetuses by the analysis of chorionic villi obtained at 9 and 11 menstrual weeks, respectively. The diagnoses were based on the absence of beta-hexosaminidase A activity as determined by: (1) specific enzyme assays, (2) anion-exchange chromatography, and (3) cellulose acetate gel electrophoresis. The enzymatic diagnoses were confirmed on fetal tissue as well as by ultrastructural demonstration of the first-trimester fetal neuropathology. Optimal assay conditions for beta-hexosaminidase A in chorionic villi were established for the prenatal diagnosis of Tay-Sachs disease. Importantly, it was noted that a small amount of decidua or maternal blood could lead to misdiagnosis. Thus, extreme care must be taken in the preparation of chorionic villi for Tay-Sachs as well as other prenatal metabolic diagnoses.
通过分别分析在妊娠9周和11周时获取的绒毛膜绒毛,对两名患病风险胎儿进行了泰-萨克斯病的产前诊断。诊断依据是缺乏β-己糖胺酶A活性,这是通过以下方法确定的:(1)特异性酶测定,(2)阴离子交换色谱法,以及(3)醋酸纤维素凝胶电泳法。酶学诊断在胎儿组织上得到证实,同时通过孕早期胎儿神经病理学的超微结构表现也得到了证实。为泰-萨克斯病的产前诊断确定了绒毛膜绒毛中β-己糖胺酶A的最佳测定条件。重要的是,注意到少量蜕膜或母体血液可能导致误诊。因此,在为泰-萨克斯病以及其他产前代谢诊断准备绒毛膜绒毛时必须格外小心。