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.
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.
Why is this test done?
Your provider may suggest an amniocentesis DNA test under the following circumstances:
What is the disorder that amniocentesis can detect?
An amniocentesis DNA test can detect the following disorders: