染色体异常是否会导致习惯性流产和胎儿停止生长发育?Can chromosomal abnormalities lead to habitual miscarriage and fetal growth cessation?

陈凤林教授指出：致死型染色体异常无法形成胚胎;致残型，无生育能力;所以，因为习惯性流产来就诊的，如果有染色体异常，也只有携带型一种可能。这种类型又不会导致习惯性流产。如果说夫妇一方有携带型染色体异常就一定流产，那么世界上岂不是没有染色体异常的人了?

Professor Chen Fenglin pointed out that: lethal chromosome abnormalities can not form embryos; disabled type, no fertility; therefore, because of habitual miscarriage, if there are chromosome abnormalities, there is only one possibility of carrying type. This type does not lead to habitual miscarriage. If a couple with a carrier chromosome abnormality must have miscarriage, then there is no chromosome abnormality in the world?

在早期自然流产时，约有50%-60%是由“胚胎”染色体异常所致。胚胎染色体异常发生的主要原因有抗胚胎抗体阳性(大于1：64)(安太专利)、宫内环境异常，如纵隔，肌瘤、息肉和内分泌异常等;其次才是孕期接触电离辐射、化学物品、微生物感染和遗传等。可以染色体异常是结果，不是病因。

About 50% to 60% of early spontaneous miscarriages are caused by chromosomal abnormalities in embryos. The main causes of chromosomal abnormalities in embryos are positive anti-embryo antibody (more than 1:64) (patented by Antai), abnormal intrauterine environment, such as mediastinum, myoma, polyps and endocrine abnormalities, etc., followed by exposure to ionizing radiation, chemicals, microbial infection and heredity during pregnancy. It is possible that chromosomal abnormalities are the result, not the cause.