NIPT With 60 MicroDeletions & Reassurance Scan

The NIPT with 60 Microdeletions process is as straightforward as a standard blood test, performed by a qualified phlebotomist for your convenience.

Your appointment includes a reassuring ultrasound scan conducted by an experienced and certified sonographer, ensuring both accuracy and peace of mind.

This advanced screening goes beyond the standard NIPT, including:

• Sex chromosomes (optional)

Additionally, it screens for specific microdeletion syndromes:

• Androgen insensitivity syndrome (AIS) • Angelman syndrome/Prader-Willi syndrome • Bannayan-Riley-Ruvalcaba syndrome (BRRS) • Branchiootorenal dysplasia syndrome (BOR)/ Melnick-Fraser syndrome • Cat eye syndrome (CES) • Chromosome 10q deletion syndrome • Chromosome 10q22.3–q23.31 microdeletion syndrome • Chromosome 18p deletion syndrome • Chromosome 18q deletion syndrome • Cornelia de Lange syndrome (CDLS) • Cowden syndrome (CD) • Cri du Chat (5p deletion) syndrome • Dandy-Walker syndrome (DWS) • DiGeorge syndrome type 2 (DGS2) • Distal arthrogryposis type 2B (DA2B) • Duchenne and Becker muscular dystrophy (DMD/BMD) • Dyggve-Melchior-Clausen syndrome (DMC) • Feingold syndrome • Holoprosencephaly type 1 (HPE1) • Holoprosencephaly type 4 (HPE4) • Holoprosencephaly type 6 (HPE6) • Jacobsen syndrome • Langer-Giedion syndrome (LGS) • Leukodystrophy with 11q14.2–q14.3 • Mental retardation, X-linked growth hormone deficiency (MRGH) • Microphthalmia, syndromic type 6, pituitary hypoplasia • Microphthalmia with linear skin defects • Monosomy 9p syndrome • Orofaciodigital syndrome • Panhypopituitarism, X-linked • Potocki-Lupski syndrome (17p11.2 duplication syndrome) • Prader-Willi-like syndrome (SIM1 syndrome) • Rieger syndrome type 1 (RIEG1) • Saethre-Chotzen syndrome (SCS) • Sensorineural deafness and male infertility • Smith-Magenis syndrome • Split-hand/foot malformation type 3 (SHFM3) • Split-hand/foot malformation type 5 (SHFM5) • Syndrome diaphragmatic hernia, congenital (HCD/DIH) • Trichorhinophalangeal syndrome type I (TRPS1) • Van der Woude syndrome (VWS) • WAGR syndrome and aniridia II • Wilms tumor 1 (WT1) • X-linked lymphoproliferative syndrome (XLP) • Xp11.22–p11.23 microduplication syndrome • 1p36 microdeletion syndrome • 1q41–q42 microdeletion syndrome • 2q33.1 deletion syndrome/Glass syndrome • 5q21.1–q31.2 deletion syndrome • 8p23.1 deletion syndrome • 8p23.1 duplication syndrome • 11q11–q13.3 duplication syndrome • 12q14 microdeletion syndrome • 14q11–q22 deletion syndrome • 15q26 overgrowth syndrome • 16p11.2–p12.2 microdeletion syndrome • 16p11.2–p12.2 microduplication syndrome • 17q21.31 deletion syndrome • 17q21.31 duplication syndrome

Who Can Take the Test?

This test is suitable for singleton pregnancies and monochorionic twin pregnancies.

Why Choose NIPT with Microdeletions?

Starting as early as 10 weeks, this simple, non-invasive screening test identifies the probable presence of:

• Down’s Syndrome
• Edwards’ Syndrome
• Patau’s Syndrome
• Including 60 Microdeletions

Plus, you have the option to learn the probable sex of your baby as part of the test.