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NIPT PLUS Genetic Fetus Test
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NIPT PLUS Genetic Fetus Test

NIPT+ performed after week 12. Analyzes cfDNA in mother's blood for trisomies 21, 18, 13, sex chromosomes, and rare trisomies/microdeletions. Safe for fetus.

Instructions Before the Test

  • Inform lab of medical conditions or blood thinners.

Sample Type

Venous blood sample.

Collection Method

Maternal venous blood draw.

Other Tests

Down Syndrome (Trisomy 21)
Extra chromosome 21.
Edwards Syndrome (Trisomy 18)
Extra chromosome 18. Serious condition.
Patau Syndrome (Trisomy 13)
Extra chromosome 13.
Turner Syndrome (45,X)
Affects females only. Missing X.
Klinefelter Syndrome (47,XXY)
Affects males only. Extra X.
Triple X Syndrome (47,XXX)
Triple X Syndrome.
XYY Syndrome (47,XYY)
Affects males. Extra Y.
Rare Trisomies
Extra chromosomes in non-common pairs.
Microdeletion Syndromes
Loss of small chromosome parts (e.g., DiGeorge).
Microduplication Syndromes
Duplication of small chromosome parts.
Baby Gender Detection
>99% accuracy.

Package Price

1,600SAR