Lowden J A, Rudd N, Cutz E, Doran T A
Can Med Assoc J. 1975 Sep 20;113(6):507-11.
In 4 years of 24 fetuses at risk for various sphingolipid and mucopolysaccharide storage diseases were examined. Amniocentesis at 16 weeks' gestation was followed in most cases by culture of amniotic fluid cells and measurement in the cells of the activity of the enzyme suspected to be deficient. Six fetuses were affected; five were examined morphologically and biochemically after abortion. Two fetuses had Tay-Sachs disease, two had GM1 gangliosidosis and one had Hurler's syndrome. Although in each affected detus the specific enzyme activity was absent, we found in the placenta 5 to 50% of the normal activity.
在4年的时间里,对24例有患各种鞘脂类和粘多糖贮积病风险的胎儿进行了检查。大多数情况下,在妊娠16周时进行羊膜穿刺术,随后对羊水细胞进行培养,并测定细胞中疑似缺乏的酶的活性。6例胎儿患病;5例在流产后进行了形态学和生化检查。2例胎儿患泰-萨克斯病,2例患GM1神经节苷脂病,1例患胡勒氏综合征。尽管在每例患病胎儿中都缺乏特定的酶活性,但我们发现胎盘中的活性为正常活性的5%至50%。