Wolstenholme J, Rooney D E, Davison E V
Department of Human Genetics, University of Newcastle upon Tyne, U.K.
Prenat Diagn. 1994 May;14(5):345-61. doi: 10.1002/pd.1970140505.
In a retrospective collaborative study involving 21 U.K. laboratories and 11,775 CVS prenatal diagnostic procedures, a total of 73 cases of confined placental mosaicism (CPM) were identified among the 8004 first-trimester referrals because of advanced maternal age, a previous child with a numerical chromosome abnormality, or a family history of the same. Data were collected on subsequent cytogenetic follow-up and pregnancy outcome for each case and a referral matched control. Comparison with the control population failed to demonstrate a marked increase in adverse pregnancy outcome in the CPM group, but a significant increase in both low and high birth weight infants was recorded. In a parallel study, 7 out of 108 cases, referred for prenatal diagnosis because of ultrasound detection of isolated intrauterine growth retardation (IUGR) in the second or third trimester, were shown to have a chromosome abnormality restricted to the extraembryonic tissues. These included cases of CPM involving trisomy 9 and del(13)(q13), neither of which has previously been reported in association with IUGR.
在一项涉及21个英国实验室和11775例绒毛取样产前诊断程序的回顾性合作研究中,在8004例因孕妇年龄偏大、曾生育过染色体数目异常患儿或有家族病史而在孕早期转诊的病例中,共识别出73例局限性胎盘嵌合体(CPM)。收集了每个病例及其转诊匹配对照的后续细胞遗传学随访和妊娠结局数据。与对照人群相比,CPM组不良妊娠结局并未显著增加,但低出生体重和高出生体重婴儿均有显著增加。在一项平行研究中,108例因超声检测到孕中期或孕晚期孤立性宫内生长受限(IUGR)而转诊进行产前诊断的病例中,有7例被证明存在局限于胚外组织的染色体异常。这些病例包括涉及9三体和13号染色体长臂1区3带缺失(del(13)(q13))的CPM病例,此前均未报道过它们与IUGR相关。