Philipp Tom, Kalousek Dagmar K
Ludwig Boltzmann Institute of Clinical Gynecology and Obstetrics, Danube Hospital, Vienna, Austria.
Am J Med Genet. 2002 Jul 22;111(1):43-7. doi: 10.1002/ajmg.10476.
A direct view of the embryo by means of transcervical embryoscopy prior to evacuation in 154 cases of missed abortion showed general embryonic maldevelopment in 48 cases (31%). A successful cytogenetic evaluation of these growth-disorganized embryos was performed in 37. Chromosomal abnormalities were found in 26 cases (70%), with autosomal trisomies in 24 cases (92%). Trisomies involved chromosome 3 (one case), 6 (one case), 8 (two cases), 10 (one case), 12 (two cases), 14 (one case), 16 (11 cases), 20 (one case), and 22 (four cases). Most of these chromosome abnormalities represented nonviable defects, and their presence explained the minimal embryonic development observed embryoscopically. An apparently normal karyotype was observed in 11 growth-disorganized embryos whose maldevelopment was similar to that resulting from the trisomies listed above. The factors responsible for embryonic maldevelopment with a normal karyotype are presently unknown and require further study, including investigation of imprinting defects, subtelomeric abnormalities, and cryptic mosaicism.
在154例稽留流产病例中,于清宫术前通过经宫颈胚胎镜直接观察胚胎,结果显示48例(31%)存在胚胎整体发育不良。对其中37例发育紊乱的胚胎成功进行了细胞遗传学评估。发现26例(70%)存在染色体异常,其中24例(92%)为常染色体三体。三体涉及3号染色体(1例)、6号染色体(1例)、8号染色体(2例)、10号染色体(1例)、12号染色体(2例)、14号染色体(1例)、16号染色体(11例)、20号染色体(1例)和22号染色体(4例)。这些染色体异常大多代表无法存活的缺陷,其存在解释了胚胎镜下观察到的胚胎发育极小的情况。在11例发育紊乱的胚胎中观察到明显正常的核型,其发育不良情况与上述三体导致的情况相似。目前尚不清楚核型正常但胚胎发育不良的原因,需要进一步研究,包括对印记缺陷、亚端粒异常和隐匿性嵌合体的调查。