PRENATAL-DIAGNOSIS OF THE INFANTILE TYPE OF NEURONAL CEROID LIPOFUSCINOSIS BY ELECTRON-MICROSCOPIC INVESTIGATION OF HUMAN CHORIONIC VILLI

被引:35
作者
RAPOLA, J
SALONEN, R
AMMALA, P
SANTAVUORI, P
机构
[1] UNIV HELSINKI,CENT HOSP,DEPT OBSTET & GYNECOL,PRENATAL GENET LAB,SF-00290 HELSINKI 29,FINLAND
[2] UNIV HELSINKI,DEPT CHILD NEUROL,SF-00100 HELSINKI 10,FINLAND
关键词
Chorionic villi; Electron microscopy; Infantile neuronal ceroid lipofuscinosis;
D O I
10.1002/pd.1970100902
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Chorionic villus biopsy specimens were studied electron microscopically in six pregnancies at risk of the infantile type of neuronal ceroid lipofuscinosis (INCL). The biopsy was performed in all cases in the first trimester of pregnancy (8–10 gestation weeks) by the transcervical route. In one case, the biopsy was repeated at 17 weeks by the transabdominal procedure. In two pregnancies, the endothelial cells and, to a lesser extent, the mesenchymal cells of the chorionic villi contained unit membrane‐bound inclusions typical of INCL. In both cases, the pregnancy was terminated and in one of them identical inclusions were found in the brains and kidneys of the fetus at 20 weeks of gestational age. The children from the remaining four pregnancies are healthy and have shown no signs of the disease. Copyright © 1990 John Wiley & Sons, Ltd.
引用
收藏
页码:553 / 559
页数:7
相关论文
共 12 条
[1]   ULTRASTRUCTURAL CHARACTERISTICS OF ABNORMAL CYTOSOMES IN BATTEN-KUFS DISEASE [J].
CARPENTER, S ;
KARPATI, G ;
ANDERMANN, F ;
JACOB, JC ;
ANDERMANN, E .
BRAIN, 1977, 100 (MAR) :137-156
[2]   1ST-TRIMESTER DIAGNOSIS OF JUVENILE NEURONAL CEROID LIPOFUSCINOSIS BY DEMONSTRATION OF FINGERPRINT INCLUSIONS IN CHORIONIC VILLI [J].
CONRADI, NG ;
UVEBRANT, P ;
HOKEGARD, KH ;
WAHLSTROM, J ;
MELLQVIST, L .
PRENATAL DIAGNOSIS, 1989, 9 (04) :283-287
[3]   INFANTILE TYPE OF SO-CALLED NEURONAL CEROID-LIPOFUSCINOSIS - HISTOLOGICAL AND ELECTRON-MICROSCOPIC STUDIES [J].
HALTIA, M ;
RAPOLA, J ;
SANTAVUORI, P .
ACTA NEUROPATHOLOGICA, 1973, 26 (02) :157-170
[4]  
JARVELA I, 1990, 3RD INT C CER LIP IN
[5]   PROBABLE EXCLUSION OF JUVENILE NEURONAL CEROID LIPOFUSCINOSIS IN A FETUS AT RISK - AN INTERIM-REPORT [J].
KOHLSCHUTTER, A ;
RAUSKOLB, R ;
GOEBEL, HH ;
ANTONLAMPRECHT, I ;
ALBRECHT, R ;
KLEIN, H .
PRENATAL DIAGNOSIS, 1989, 9 (04) :289-292
[6]  
MacLeod P M, 1988, Am J Med Genet Suppl, V5, P93
[7]   PRENATAL-DIAGNOSIS OF NEURONAL CEROID-LIPOFUSCINOSES [J].
MACLEOD, PM ;
DOLMAN, CL ;
NICKEL, RE ;
CHANG, E ;
NAG, S ;
ZONANA, J ;
SILVEY, K .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 22 (04) :781-789
[8]  
RAPOLA J, 1988, American Journal of Human Genetics, V43, pA245
[9]  
Rapola J, 1988, Am J Med Genet Suppl, V5, P99
[10]   SUCTION BIOPSY OF RECTAL MUCOSA IN THE DIAGNOSIS OF INFANTILE AND JUVENILE TYPES OF NEURONAL CEROID LIPOFUSCINOSES [J].
RAPOLA, J ;
SANTAVUORI, P ;
SAVILAHTI, E .
HUMAN PATHOLOGY, 1984, 15 (04) :352-360