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UE3 is a highly specific marker of pregnancy, barely detectable in non-pregnant or males, and is synthesized primarily in the fetal-placental complex.
The concentration of UE3 in fetal serum increases with gestational age. Its concentration is about 5 times that of the maternal serum concentration. Maternal serum levels of UE3 begin to exceed non-pregnant levels at 7 to 9 weeks gestation and then continue to rise, peaking before term.
Maternal serum UE3 levels in mothers pregnant with Down syndrome were on average 29% lower than normal pregnancy levels.
The information of the pregnant woman should be checked first, the date of birth of the pregnant woman (solar calendar), weight (fasting net weight), gestational age (generally calculated by ultrasound fetal double top diameter or head and hip diameter, and the gestational age may not be reliable according to the last menstrual period), if there is no error in these important information, you can consider doing amniocentesis examination, if the information is wrong, you should recheck. The true fetus of high-risk pregnant women is only 1,100, so there is no need to be nervous.
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As long as the left ventricular bright spot does not exceed 1 cm, there is no need to be nervous, which may be caused by calcification spots in the ventricle.
Suggestions: You can observe at any time, and recheck it in a week to see if there is any change in the calcification point. In general, most of them are physiological.
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As long as trisomy 21 is low-risk, there is no need to wear sheep.
Sheep wearing not only carries the possibility of infection, but also increases the risk of miscarriage.
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Hello, did you later do sheep wear or non-invasive? What is the result My situation is the same as yours It is also a low UE3MOM value 2 strong light spots in the four-dimensional left ventricle The doctor asked the sheep to wear or non-invasive.
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Judging from your examination results, this normal and abnormal is directly about the same, so that the situation will not have adverse effects, that is to say, the possibility of Down syndrome is relatively small, because a simple result is abnormal, and the difference between the normal and abnormal values is relatively small, so you can rest assured, and it is recommended to review the ultrasound regularly, so that you can dynamically observe the development of the fetus.
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Judging from your test results, this normal and abnormal are directly about the same, so there will be no adverse effects, that is to say, the possibility of Down syndrome is relatively small, because the simple result is abnormal, and the difference between the normal and abnormal values is relatively small, so you can rest assured.
At the same time, it is recommended to have regular follow-up ultrasound, so that the development of the fetus can be dynamically observed.
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Down's screening is already low-risk, which means that there is no problem, and you are so close, you don't have to do a puncture, you have to believe in yourself, and from AFP and HCG, you have a great chance of being pregnant with a baby girl. It is recommended not to believe the doctor's scare, amniocentesis has a 1% chance of miscarriage, do not do it lightly.
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Alpha-fetoprotein (AFP) and other indicators are normal, and UE3 is a little low, the risk is so low, there is no need for puncture. Of course, it may be that the doctor is afraid of accidents, it is safer to do a puncture, and if you are also worried about accidents, just listen to the doctor, there is no danger or harm to the child (provided that it is a regular hospital).
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You are all low-risk, there is really no need to do it, you only have UE3 This item is a little low, it doesn't matter, you can do a four-dimensional color ultrasound at 20-24 weeks to see the development of various organs of the fetus, and rule out malformations.
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Hello, has your baby been born? I said that UE3 is low, does it have any effect, thank you.
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It's a low-risk report, which means that your child's chances of getting this disease are very low, okay!!
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Hello! Many pregnant women at high risk of Down syndrome have undergone amniocentesis or genetic diagnosis, and the baby is healthy, and the low-risk pregnant women also have sick children; Non-invasive genetic diagnosis of children with Down syndrome is a new means to diagnose Down's syndrome, which not only improves the detection accuracy of chromosomal diseases, but also effectively avoids the risk of amniocentesis and greatly improves the health and safety factor of the fetus, which is a detection method worth advocating.
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If there are some problems, it is better to listen to the doctor's advice and do a follow-up.
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Hello, happy to answer your questions. It doesn't matter, if it's just this one of the high risks, it should be fine.
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AFP should be clinically meaningful when Bisen combines the value of HCG, and the single item is that there is no significant AFP reduction, HCG increase, combined with B-ultrasound examination and analysis, before considering that the fetus has a mountain problem.
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Me too, the doctor said that this reaction placental function, low is not so good.
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Low risk is safe, and there will be no possibility of Down's.
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You should take the report to the doctor.
Children with Down syndrome have severe intellectual disability, are unable to take care of themselves, and are accompanied by complex cardiovascular diseases, which require long-term care from their families, which will cause great mental and financial burden to their families. >>>More
It must be done, although amniocentesis has an effect on the fetus, but within the acceptable range, the lesser of two evils. If you don't do it, no one knows what the outcome will be, and if there is a result that you don't want to see, it's too late to regret it.
Judging from the data of the test list, it is low-risk, but the current general serological Tang screening has great shortcomings, the accuracy rate is not very high, and the false positive rate is also very high. Invasive tests such as amniocentesis carry a high risk and can lead to miscarriage. >>>More
If necessary, it is recommended to listen to the doctor's advice to go back for a follow-up.
The purpose of hearing screening for newborns is to avoid congenital hearing loss, and secondly, if the newborn is affected by medication during pregnancy or because of the virus, the newborn's hearing loss can be detected earlier through hearing screening, and it can also be carried out earlier**. It has been medically confirmed that babies within 3 years of age are the best time for hearing loss, and it is even better if the baby's hearing loss is found after 6 months of birth and given ****. Therefore, the earlier the baby's hearing loss is detected, the sooner it can be, and this can maximize the level of language development of children with hearing loss to the greatest extent close to and reach the same age.