Amniocentesis DNA Test

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Amniocentesis DNA Test

Amniocentesis DNA Test

Welcome to a guide for New York DNA testing for amniocentesis and find out if there is any kind of potential health risk that your baby might suffer with. This guide is created to help you with the process of the Amniocentesis DNA Test and solve any kind of query related to the topic. So let’s dive right into it,

What is amniocentesis?

An amniocentesis DNA test is a prenatal diagnosis that is used to detect if your baby has any kind of genetic disorder, neural tube defects, or abnormal chromosomal number which can cause disorders like Down syndrome, Edward’s syndrome, Patau’s syndrome, spina bifida, etc in the fetus during the pregnancy.

This test is performed between 15-20 weeks of gestation and can provide valuable information about your baby’s health. And also gives you time to prepare in advance if the results come out abnormal.

Amniocentesis DNA Test

How is an amniocentesis DNA test performed?

During an amniocentesis DNA test, the doctor inserts a thin needle in the uterus to obtain a small amount of amniotic fluid from the sac surrounding the fetus. The amniotic fluid collected is used as a sample to conduct the test in the laboratory to look for genetic conditions and other kinds of potential issues that might cause harm to your child’s health.

Procedure:

  • Firstly the doctor will use an antiseptic to clean a small area of your abdomen.
  • Then they will apply a specific gel to your stomach.
  • The doctor then uses an instrument over the gel to collect ultrasound images of the fetus, and observe the images displayed on a nearby monitor.
  • Then the slender, hollow needle is inserted into the abdomen and uterus which is used to remove a small amount of amniotic fluid.
  • After the needle is removed the ultrasound monitors your baby’s heartbeat and activity to confirm that they were not impacted by the process.
  • Following the procedure, your healthcare professional sends the amniotic fluid sample to a laboratory for analysis.

 

 

Amniocentesis DNA Test

Why is this test done?

Your provider may suggest an amniocentesis DNA test under the following circumstances:

  • Your ultrasound test showed abnormality in the fetus.
  • The prenatal screening test showed the probability of abnormal chromosomes.
  • If you have a family history of genetic disorders.
  • If you are pregnant after the age of 30-35 years because after this age the chances of the baby getting a genetic disorder increases.

What is the disorder that amniocentesis can detect?

An amniocentesis DNA test can detect the following disorders:

  • Birth defects like spina bifida
  • Genetic disorders like Down syndrome or Patau syndrome.
  • Lung development of the unborn child.
  • Other potential health concerns like Rh disease.
  • Amniocentesis can also help with polyhydramnios to remove the extra amniotic fluid.

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