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Microscope

Prenatal Screening Panels

Non-invasive Prenatal Screening 1 - NIFTY

Screening of trisomies and sex chromosome aneuploidies

Trisomies 

  1. Trisomy 21

  2. Trisomy 18

  3. Trisomy 13

Sex Chromosome Aneuploidies

  1. Monosomy X (X0)

  2. XXY

  3. XXX

  4. XYY

Specimen Requirements

  • Maternal peripheral blood in STRECK tube (Special collection kit, please request from laboratory)

LAT (Laboratory turnaround time)

  • 10 - 14 working days

Non-invasive Prenatal Screening 2 – NIFTY Pro

Screening of trisomies, rare autosomal
aneuploidies, sex chromosome aneuploidies, microdeletions/duplications and incidental findings

Trisomies 

  1. Trisomy 21

  2. Trisomy 18

  3. Trisomy 13

Rare Autosomal Aneuploidies 

  1. Trisomy 9

  2. Trisomy 16

  3. Trisomy 22

Sex Chromosome Aneuploidies

  1. Monosomy X (X0)

  2. XXY

  3. XXX

  4. XYY

Specimen Requirements

  • Maternal peripheral blood in STRECK tube (Special collection kit, please request from laboratory)

LAT (Laboratory turnaround time)

  • 10 - 14 working days

NEOGENIX LABORATOIRE SDN BHD

Unit C707 Level 7
Block C Kelana Square
17 Jalan SS7/26 Kelana Jaya
47301 Petaling Jaya
Selangor Darul Ehsan
Malaysia

☏ +603 7621 2154

 
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Neogenix Laboratoire performs laboratory testing for all patients and does not discriminate based on race, color, national origin, sex, age, disability or gender identity.

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201601021028 (1191967-W)
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