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Are you going to have a genetic test with blood or serious intervention? You need to decide which one you want if you want to know exactly if you are looking for a healthy baby. We summarized the essence.
"Genetic" ultrasound: risk assessment12-14. In the case of weekly ultrasound, it is of particular importance that the examiner is appropriately qualified and experienced by a doctor or sonographer. With a lot of unnecessary worry, parents are trained by the eyes and precision to measure the thickness of the fetus's tailbone and see if its nostrils are visible.
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Down kуrplayback The average lobe thickness (NT in the find) is 1.5 millimeters for healthy fetuses and the limits are 3 millimeters. In other words, it is very small distances to recover, where tenth of a millimeter is a big difference. 5-10 percent of healthy people have thicker bone at the average and at the border, but this symptom can also be a symptom of Down syndrome, along with nasal deficiency. It is also possible that all measured data are in the normal range, the nasal bone (NB in the finding) can be seen, as well as Down Syndrome, since it is not a diagnostic test, only a risk assessment.
Combined test: This is also a screening test
Pregnant women whose pregnant caregiver performs 12-14 can get it free of charge. weekly ultrasound with a suitably qualified specialist and a contract with Sejtbank Ltd., which provides free blood tests - that is, social security is only cleaning the ultrasound. You can take advantage of any of your pregnant mothers' salaries in private, and you can expect to have the results in another country, as well as in other cases for up to a week.Szбmoljunk! What does the result mean?
It varies by genetic center what ratio (1: 150, 1: 250, 1: 380) is considered as the limit between positive and negative cases. The point is to give the currency that a baby with the same result turns out to be fetal mumps with Down syndrome. That is, if you put your personal risk at a ratio of 1: 250, that means that 250 will have the same result for a proven Down course in a genetic test. For example, a 1: 100 result is positive, but it just means that out of a single genetic test, only one out of every 99 actually shows an abnormality, the other 99 are negative for a genetic test.
It should also be borne in mind that, with the age of the mother over 40, the chances of having a negative outcome in any of several factors are decreasing. This is the explanation for the fact that among young people, the positive results are fewer, but older people are more frequent. Starting at 3.2-3.4, it is virtually inconceivable that the value of biochemical markers be such that the result falls within the negative range.
Are you coming?
At www.sejtbank.hu you can check the list of Sejtbank Kft. Partners to see if your doctor or doctor is among you. On www.gendiagnoszika.hu, you can review the combined screening conditions for pay, while under another umbrella, and the lupus biopsy (chorionic biopsy), which gives you no risk but an estimate.
Important difference: screening or diagnosis
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Time factor, ie when will the result be?
"We prefer the combined test" - say many babies over thirty because they don't want "abdominal cleansing". However, you are curious as to what the test result will be. After all, it will be negative with the greatest currency, and it can be very reassuring for the remaining six months of pregnancy. But what do you mean by a 1: 100 (positive) result? When you make a decision, also consider when your filter results are. If this is positive, and for this reason will a genetic test be suggested, when will it be successful?
If the fetus is ill, how many weeks will you face the final choice? If you vote for the combined test and the puffer test - then you can go from 13-14. every week you get a final answer. If you omit this opportunity, you can go around the twentieth week to get the good or bad news. By then, you're over the baby killing. Professionals therefore strongly recommend that you carry out an earlier examination.
Which exams are many?It is possible that you have missed a combined test for a variety of reasons and are already pregnant or 14 weeks pregnant when you decide to have a screening test. What are your options? Of course, these are all paid exams with the AFP exception: here you can check out where they are: www.gendiagnosztika.hu, www.downszures.hu, www.g1intezet.hu, www.medicover.hu
AFP: Examines the presence of fetal white in the mother's blood. In some cases, low AFP may refer to Down's lobe, and high values may indicate open spine or cerebral palsy. Alternatively, in some laboratories, the value of another marker, the beta-HCG, is also being tested for social security purposes, as this increases the very low probability rate. Different AFP values from the average are not in themselves a reason for an amniotic fluid test.
Quartet Test (quadruple test): Performs between the 16th and 19th weeks to test for tracer levels, including AFP and Beta-HCG.
Sequence analysis: the combined test and quadruple test are combined, thus further refining the results of the combined test.
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