Genetic Testing During Prenatal Testing Uncovers Rare Autosomal Trisomies

Prenatal testing is used to determine if the unborn baby is healthy inside the womb. It helps detect birth defects and genetic diseases in the baby before birth. Most pregnant mothers prefer non-invasive testing like blood tests rather than the invasive procedures like amniocentesis where fluid is taken from the amniotic sac.

Genetic testing of all 46 chromosomse detects rare autosomal trisomies (RATs)
RAT associated with
- early miscarriage
- in-utero fetal death
- intrauterine growth restriction of fetus

Genetic Testing During Non-invasive Prenatal Testing Uncovers Rare Autosomal Trisomies

Noninvasive prenatal testing including all 23 pairs of chromosomes discovers rare trisomies that suggest feto-placental diseases and miscarriages. Read More

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Prenatal Screening Test

Prenatal screening involves various tests to assess the risk of the unborn baby to be born with a chromosomal anomaly, neural tube defect or any birth defect.

Genetic Testing Procedure

In most cases genetic testing is done using blood samples. Other tissues and body fluids like skin, hair, bone marrow, amniotic fluid and semen are also employed

Prenatal Screening Test - Frequently Asked Questions

Do you know which doctor should you consult for Prenatal Screening Test. This and other commonly asked questions about this condition.

Non-Invasive Prenatal Genetic Test is Accurate Five Weeks into Pregnancy

Trophoblast Retrieval and Isolation from the Cervix (TRIC) - offers the accuracy of more invasive tests, such as the needle-directed amniocentesis.

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