What is this test?
A combination of screening and diagnostic tests on maternal or fetal samples.
When is this test recommended?
Across pregnancies, especially in higher-risk or family-history cases.
Sample type
Maternal blood, amniotic fluid, CVS.
Results
Assessment of aneuploidies, monogenic diseases and structural anomalies.
Limitations
Invasive procedures carry miscarriage risk; screening tests are not definitive.
Turnaround time
To Be Added
Required documents
To Be Added
Related diseases
Aneuploidies, thalassemia, SMA, DMD.