Zerres K, Schüler H, Gembruch U, Bald R, Hansmann M, Schwanitz G
Institut für Humangenetik Universität, Bonn, Federal Republic of Germany.
Hum Genet. 1992 May;89(3):301-4. doi: 10.1007/BF00220545.
Choroid plexus cysts were diagnosed in 25 out of 823 fetuses with prenatally diagnosed abnormalities (growth retardation/malformations). Among these, 5 revealed a chromosomal disorder (4 cases with trisomy 18 and one case with a translocation trisomy 21). Additional abnormalities, such as growth retardation, holoprosencephaly, hydrocephalus and club foot, were found in 6 out of the 20 fetuses with no chromosomal abnormality. All fetuses with a chromosomal disorder revealed further typical prenatally recognizable abnormalities. Our observation indicates that prenatally diagnosed choroid plexus cysts should be considered as an indication for prenatal chromosomal diagnosis, although the risk of there being an underlying chromosomal disorder is low in cases with no additional abnormalities.
在823例产前诊断为异常(生长迟缓/畸形)的胎儿中,有25例被诊断出脉络丛囊肿。其中,5例显示染色体异常(4例18三体综合征和1例21号染色体易位三体综合征)。在20例无染色体异常的胎儿中,有6例发现了其他异常,如生长迟缓、前脑无裂畸形、脑积水和马蹄内翻足。所有染色体异常的胎儿均显示出进一步典型的产前可识别异常。我们的观察表明,尽管在无其他异常的情况下存在潜在染色体疾病的风险较低,但产前诊断出的脉络丛囊肿仍应被视为产前染色体诊断的指征。