Wiesmann U N, Meier C, Spycher M A, Schmid W, Bischoff A, Gautier E, Herschlowitz N
Helv Paediatr Acta. 1975 May;30(1):31-42.
In a family with a metachromatic leukodystrophy patient, two further pregnancies at risk were monitored by amnion cell culture. In one case, a normal baby was predicted and born. In the other case, a prenatal deficiency of arylsulfatase A was found. The diagnosis of metachromatic leukodystrophy was confirmed biochemically in various organs of the fetus by the deficiency of arylsulfatase A. The residual enzyme activity was shown to have an abnormal pH optimum and an increased heat stability. Ultrastructural studies revealed lipid storage in the myelinating nervous system and in the liver. For the interpretation of morphological results, it was indispensable to analyze an age-matched control fetus.
在一个患有异染性脑白质营养不良症患者的家庭中,对另外两次有风险的妊娠进行了羊膜细胞培养监测。其中一例预测并出生了一个正常婴儿。另一例则发现产前芳基硫酸酯酶A缺乏。通过芳基硫酸酯酶A缺乏在胎儿的各个器官中进行生化确认,诊断为异染性脑白质营养不良症。残留酶活性显示具有异常的最适pH值和增加的热稳定性。超微结构研究揭示了在有髓神经系统和肝脏中的脂质蓄积。为了解释形态学结果,分析年龄匹配的对照胎儿是必不可少的。