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Medicinal services suppliers can check for Down syndrome during pregnancy or after a kid is conceived. There are two sorts of tests for Down syndrome during pregnancy:

 

  • A pre-birth screening test. This test can demonstrate an improved probability that a baby has Down syndrome, yet it can’t decide متلازمة الداون is certainly present. In the event that a screening test demonstrates an improved probability, an indicative test can be requested.
  • A pre-birth symptomatic test. This test can decide with an assurance that Down syndrome is available. Analytic tests convey a marginally more serious hazard to the embryo than do screening tests.

 

The American Congress of Obstetricians and Gynecologists (ACOG) suggests that every pregnant lady be offered a Down syndrome screening test.

 

Pre-birth Screening for Down Syndrome

 

There are a few choices for Down syndrome pre-birth screening. These include:

 

  • A blood test and an ultrasound test during the primary trimester of pregnancy. This is the most acknowledged methodology for screening during the main trimester. A blood test empowers a medicinal services supplier to check for “markers, for example, certain proteins, in the mother’s blood that propose an improved probability of Down syndrome. Then the social insurance supplier completes an ultrasound test, which uses high-recurrence sound waves to make pictures. An ultrasound can distinguish liquid at the back of an embryo’s neck, which here and there demonstrates Down syndrome. The ultrasound test is called the estimation of nuchal translucency. During the principal trimester, this consolidated strategy results in more powerful or tantamount location rates than strategies utilized during the second trimester.
  • A blood test during the second trimester of pregnancy. As in the primary trimester, a blood test empowers a social insurance supplier to check for markers in the mother’s blood. A triple screen searches for dimensions of three unique markers; a fourfold screen searches for dimensions of four distinctive markers.
  • A joined test (in some cases called a coordinated test). This methodology utilizes both a blood test and an ultrasound during the principal trimester just as a moment trimester blood test. Social insurance suppliers at that point consolidate every one of these outcomes to deliver one Down syndrome hazard rating.

 

On the off chance that a lady is pregnant with twins or triplets, a blood test won’t be as dependable in light of the fact that the substances from a Down syndrome embryo might be more earnestly to detect.

 

Pre-birth Diagnostic Testing for Down Syndrome

 

In the event that a screening test recommends the probability of Down syndrome, a demonstrative test can be performed. ACOG prescribes that pregnant ladies of any age be given the choice of avoiding the screening test and getting an indicative test first. As of not long ago, just ladies over age 35 and others in danger ladies were offered this choice in light of the fact that symptomatic tests convey a slight danger of miscarriage. Before having indicative testing, a pregnant lady and her family might need to meet with a hereditary guide to examine their family ancestry and the dangers and advantages of testing in their particular circumstance.

 

Indicative testing for Down syndrome includes evacuating an example of hereditary material. After it is expelled, the example is checked for additional material from chromosome 21, which may demonstrate that a hatchling has Down syndrome. Guardians generally get the aftereffects of the test up to 14 days after the fact. The accompanying methodology is utilized to concentrate on tests.

 

  • Amniocentesis (articulated am-nee-goodness sen-TEE-sister). A medicinal services supplier takes an example of amniotic (articulated am-nee-OT-ik) liquid, which is then tried for the additional chromosome. This test is impossible until week 14 to 18 of the pregnancy.
  • Chorionic villus (articulated KOHR-ee-on-ik VIL-uhs) examining (CVS). A human services supplier takes an example of cells from a piece of the placenta (articulated pluh-SEN-tuh), which is the organ that associates a lady and her baby, and after that tests the example for the additional chromosome. This test is done between weeks 9 and 11 of pregnancy.
  • Percutaneous (articulated pur-kyoo-TEY-nee-uhs) umbilical blood examining (PUBS). A medicinal services supplier takes an example of fetal blood in the umbilical line through the uterus. The blood is then tried for the additional chromosome. Bars is the most exact analytic strategy and can affirm the aftereffects of CVS or amniocentesis. Be that as it may, PUBS can’t be performed until some other time in the pregnancy, during the eighteenth to 22nd week.
  • Pre-birth symptomatic testing involves some hazard to the mother and baby, including a slight danger of miscarriage. If you and your family are thinking about pre-birth demonstrative testing for Down syndrome, examine every one of the dangers and advantages with your human services supplier.

 

Chromosomal Testing of Maternal Blood

 

A pregnant lady who is in danger for having a newborn child with Down syndrome additionally can have a chromosomal test utilizing her blood. A mother’s blood conveys DNA from the embryo, which may demonstrate additional chromosome 21 material.3 A progressively intrusive test at that point would normally affirm the blood test.

 

Testing and In Vitro Fertilization

 

Another way to deal with determination is utilized related to in vitro preparation. Preimplantation hereditary analysis (PGD) enables clinicians to recognize chromosome uneven characters or other hereditary conditions in a prepared egg before it is embedded into the uterus.

 

This strategy is valuable for the most part for couples who are in danger of passing on an assortment of hereditary conditions, including X-connected disarranges, just as couples who have endured repeated unconstrained pregnancy misfortunes, sub-rich couples, or those in danger for the single-quality issue.

 

Those inspired by PGD ought to have hereditary guiding and ought to think about close observing and extra testing during their pregnancies, given some expanded danger of chromosomal irregularities emerging optional to the in the vitro preparation process.

 

Analysis of Down Syndrome After Birth

 

An analysis of Down syndrome after birth is regularly founded at first on physical indications of the syndrome.

 

But since people with Down syndrome might not have these indications, and on the grounds that a large number of these side effects are normal in the all-inclusive community, the social insurance supplier will take an example of the child’s blood to affirm the finding with the help of fertility centers for best gender selection. The blood test is dissected to decide the number of the infant’s chromosomes.

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