Test Name:
Panorama Extended Screening, including 5 Microdeletions
Specialised Test:
No - Send Out Test
Additional Test Note:
Non-invasive prenatal screening test for:
Trisomy 21, Trisomy 18, Trisomy 13, Monosomy X, Triploidy, 22q11.2 deletion syndrome
(DiGeorge/ Velocardiofacial Syndrome), 1p36 syndrome, Cri du chat syndrome (5p-), Angelman
syndrome (15q11.2 deletion maternal), Prader-Willi syndrome (15q11.2 deletion paternal) and
optional gender reporting.
Trisomy 21, Trisomy 18, Trisomy 13, Monosomy X & Triploidy plus 5 microdeletions: 22q11.2 deletion (DiGeorge), 1p36 deletion, Cri-du-chat, Prader-Willi & Angelman deletions.
Sample Requirement:
2 x 10ml Whole blood (Maternal) in DNA Streck tubes provided in the Panaroma collection kit
Parkway Laboratory Services