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Tag Non-invasive prenatal screening
Articles in Non-invasive prenatal screening
Extracellular DNA screening test
Cell-free DNA screening is known as a non-invasive prenatal screening method with no risk of miscarriage, with a high disease detection rate and low false positive and false negative rates compared to traditional serum screening methods.
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How to view Double test test results
Double test prenatal screening test is used to screen for some genetic syndromes in the fetus. Knowing how to read the Double test results correctly will help parents better understand the health status of the fetus.
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Pregnant women: Who should perform the NIPT test to detect Turner syndrome in the fetus?
Turner syndrome is the most common sex chromosome disorder in women, causing a high rate of miscarriage, and the children born also have many incurable developmental disorders. To prevent the birth of children with Turner syndrome, high-risk pregnant women are advised to have prenatal screening tests.
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Effects of Edward's syndrome on the fetus
Edward syndrome is a rare genetic disorder that affects babies. Children with Edward syndrome are unlikely to survive after birth and, if they are lucky enough to be born, will develop abnormally. It is the second most common syndrome, after Down syndrome, with a rate of 1/3,000 to 1/8,000 newborns affected.
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Mechanism of Turner syndrome
Turner syndrome is the most common sex chromosome disorder in women, caused by a disorder of part or all of the X sex chromosome in the genome. The mechanism causing Turner syndrome is of interest to many scientists, clarifying it to effectively prevent this syndrome.
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What to do if the nuchal translucency measurement result is abnormal
Measuring nuchal translucency is a necessary and very important task in monitoring the development of the fetus. Usually in the 11th-14th week of pregnancy, the pregnant mother will be instructed by the doctor to measure nuchal translucency. Based on the results of the nuchal translucency measurement, the doctor will make a diagnosis of the condition of the fetus. If the results are abnormal,
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Timing of amniocentesis and chorionic villus biopsies in prenatal diagnosis
Prenatal diagnostic tests are tests that help doctors know for sure whether the fetus has genetic abnormalities and infections. Usually these tests are based on amniocentesis and chorionic villus sampling. After having the results of prenatal genetic diagnosis, parents can decide to terminate the pregnancy or consult a doctor.
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Pre-pregnancy screening and testing
To ensure a smooth pregnancy and childbirth process, minimizing possible risks, pre-pregnancy screening and testing is extremely important. When performing pre-pregnancy screening, couples need to follow the doctor's instructions to obtain accurate results, creating conditions for a successful pregnancy.
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Genetic counseling in medical care
Genetic counseling is a medical counseling process that aims to help individuals, couples or families understand and accept the medical, psychological, family-social relationship problems and the impact on the next generation caused by genetic diseases.
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