NIPT (Non-Invasive Prenatal Test)

NIPT is a screening test that can provide information on the risk of genetic abnormalities in the fetus. This examination can be performed on pregnant women from 10 weeks of pregnancy.

What can be detected through NIPT?

Trisomy 13 (Patau Syndrome) Trisomy 18 (Edward Syndrome) Trisomy 21 (Down Syndrome) Aneuploidi kromosom seks, misalnya 45, X (Turner Syndrome) Jenis kelamin janin (XX atau XY).

Advantages of NIPT

Safe and non-invasive

Sampling of the mother's blood to screen for fetal chromosomal abnormalities without harming the future baby.

The most comprehensive genomic technology

Menggunakan teknologi Whole Genome Sequencing untuk membaca susunan genomik janin secara komprehensif sehingga memberikan hasil yang akurat dan terpercaya.

Early detection

This examination can be performed from 10 weeks of pregnancy.

Tim Dokter Genetika Klinik :

Dr. dr. Lydia Pratanu, MS

Dr. dr. Nurin Aisyiyah Listyasari, M.Si.Med