Prequel NIPT Monogene Advance
Combines the maximum chromosomal screening (Karyo Advance) with complete monogenic disease detection.
Complete Detection Includes:
All sex chromosome conditions
Genome-wide CNVs >7Mb across all chromosomes
23 clinically significant microdeletions <1Mb
50 dominant/de novo monogenic diseases
52 recessive fetal monogenic diseases
Additional info:
Clinical Advantage
This test provides the most comprehensive fetal genetic risk assessment available from maternal blood alone, detecting:
- Hundreds of chromosomal abnormalities at 1Mb resolution
- Over 100 single-gene disorders (both inherited and new mutations)
- Conditions affecting every major organ system
- Both common and ultra-rare genetic diseases
Ideal for:
Patients seeking maximum prenatal information, high-risk pregnancies, complex family histories, consanguinity, or when comprehensive fetal genetic assessment is desired.
See Prequel NIPT Karyo Advance and Prequel NIPT Monogene for detailed condition descriptions.
