Källén B, Cocchi G, Knudsen L B, Castilla E E, Robert E, Daltveit A K, Lancaster P L, Mastroiacovo P
Department of Embryology, University of Lund, Sweden.
Teratology. 1994 Nov;50(5):322-31. doi: 10.1002/tera.1420500503.
The goal of this study, based on information collected from eight congenital malformation registry programs around the world, was to analyze sex and twinning of affected infants and fetuses, according to type of neural tube defect (NTD) and other variables. The type of defect and its location, whether it occurred in isolated form or was associated with other malformations, population from which data were retrieved, vital status of the infant, and gestational age of the fetus/infant were considered. The material included 3,416 infants and 168 selectively aborted fetuses with anencephaly, 4,830 infants and 76 fetuses with spina bifida, and 1,022 infants and 19 fetuses with encephalocele. Less than 20% of infants with anencephaly or spina bifida and more than one-third of infants with encephalocele had associated malformations. A female excess was found among all infants with NTD but a male excess in fetuses delivered spontaneously before week 20, indicating selective male late fetal deaths. Sex ratio varied by type of NTD, vital status at birth, presence of associated malformations, and year of birth, with an increasing sex ratio for anencephaly during the 1960s and 1970s. Twinning was positively associated with NTD but the extent of this association varied with NTD type and program, while the distribution by sex type of pair of twin appeared to be similar to that of all births. Twins concordant for anencephaly or encephalocele were mainly found when the defect occurred as part of a syndrome, and only in like-sexed pairs. Twins concordant for spina bifida had the isolated form of the defect and 5 of 6 pairs were like-sexed.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究基于从全球八个先天性畸形登记项目收集的信息,旨在根据神经管缺陷(NTD)类型和其他变量,分析受影响婴儿和胎儿的性别及双胎情况。研究考虑了缺陷类型及其位置、是否以孤立形式出现或与其他畸形相关、数据来源人群、婴儿的生命状态以及胎儿/婴儿的孕周。材料包括3416例无脑儿婴儿和168例选择性流产的无脑儿胎儿、4830例脊柱裂婴儿和76例脊柱裂胎儿,以及1022例脑膨出婴儿和19例脑膨出胎儿。无脑儿或脊柱裂婴儿中不到20%以及脑膨出婴儿中超过三分之一伴有相关畸形。在所有患NTD的婴儿中发现女性居多,但在20周前自然分娩的胎儿中男性居多,表明男性胎儿晚期选择性死亡。性别比因NTD类型、出生时的生命状态、是否存在相关畸形以及出生年份而异,在20世纪60年代和70年代无脑儿的性别比呈上升趋势。双胎与NTD呈正相关,但这种关联的程度因NTD类型和项目而异,而双胎的性别分布似乎与所有出生情况相似。无脑儿或脑膨出的双胎一致型主要在缺陷作为综合征的一部分出现时发现,且仅在同性双胎中出现。脊柱裂双胎一致型具有孤立的缺陷形式,6对中有5对是同性。(摘要截短至250字)