How Much Protein Should A 10 Month Old Baby Eat Down Syndrome – High Risk Mothers And Early Detection

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Down Syndrome – High Risk Mothers And Early Detection

As a mother-to-be, make sure you keep all doctor’s appointments, take all prenatal vitamins and supplements, and be absolutely certain to start taking care of your child as soon as you learn that you are pregnant. Prenatal care is essential for any pregnant woman. Down syndrome, as a primary concern for pregnant women over 35 or women genetically predisposed to giving birth to a child with this condition, can sometimes be detected as early as the first trimester. Please see your doctor regularly and as soon as possible for an ultrasound.

Although there is not yet much that advanced medicine can do to prevent this troubling disease, there are ways for a woman and her family to prepare to care for a child with Down Syndrome. Down. This, of course, applies to many potential pregnancies and birth defects, such as trisomy-18 and other chromosomal abnormalities that may occur. Taking care of yourself during your pregnancy is the most important thing you can do.

Every pregnancy is important and there are certainly many variables worth considering during those crucial months before the birth of your child. Whether it has already been determined to be a high risk pregnancy or whether it is a high risk pregnancy, even if (to the best of your knowledge) you and your baby are perfectly healthy , medical attention is essential as early as possible in your pregnancy.

One very important thing to do, in addition to all other prenatal care, is to get ultra-screened during your first trimester. An ultra-screen is a procedure that has been widely studied. Screening is recommended for all pregnant patients, not just women over 35. Of all Down syndrome pregnancies, 91% can be detected using an ultra-screen during the first trimester. However, there is a 5% chance of getting a false positive result. Therefore, if the first ultra-screen is positive, reschedule another one to be sure. If the screening detects a Trisomy-18 defect, it is likely to be accurate. The false positive rate on the ultra-screen for Trisomy-18 is more like one percent. The ultra screen can detect Trisomy-18 risks incredibly early with an accuracy of up to 98%.

So, some of you expectant moms-to-be are probably wondering, how exactly does the ultra-screen test go? A combination of ultrasound and blood sampling is the key to this procedure and the accuracy of its results. According to experts who regularly use the equipment, “the test begins with an ultrasound between 11w1d and 13w6d gestation.” The CRL must be between 45 and 84 mm. CRL is measured for accurate pregnancy dating (i.e. date of conception) and nuchal translucency (NT) is also measured before the procedure can be performed. NT is a specific marker for chromosomal aneuploidy that can be detected by this procedure. At the time of the ultrasound exam, doctors will take a sample of dried blood from the fingertip.

Along with the dried blood sample taken, the ultrasound data is entered on the test request form and sent to the labs for complete analysis. The blood sample is tested for free beta HCG and plasma protein A (PAPP-A), a plasma protein associated with pregnancy. The risk of trisomy 21 in the fetus as well as the risk of trisomy-18 are calculated according to the patient’s age, nuchal translucency, as well as freebeta and PAPP-A. Despite the sometimes difficult medical jargon to master, get the ultra-screen during your first trimester and ask your doctor specific questions, no matter how much you don’t understand. The number one goal is to understand as much as possible when it comes to your unborn child.

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