Prenatal diagnosis

Amniotic Fluid Chromosomal
Analysis (13,18 ,21, X&Y )

Amniotic fluid chromosome analysis is
a medical procedure used in prenatal
diagnosis of chromosomal abnormalities
and foetal infections.

NIPT

Non-invasive prenatal testing (NIPT) is a method
used to determine the risk for the fetus being born
with certain chromosomal abnormalities.

NIPT Pro

non-invasive prenatal test that analyzes
cell-free fetal DNA in maternal blood to
screen for chromosomal abnormalities
like trisomy 21, 18, and 13. It offers high
accuracy and early detection without
risk to mother or baby.

NIPT Mono

screens for Monosomy X (Turner syndrome) by analyzing cell-free fetal DNA to detect missing X chromosome abnormalities.

Amniotic Fluid Chromosomal Microarray

detects submicroscopic chromosomal abnormalities in the fetus using DNA
from amniotic fluid.

Digital Karyotyping

detects submicroscopic chromosomal abnormalities in the fetus using DNA
from amniotic fluid.

Whats app & Calls
(+20) 120 583 0835
(+20) 102 152 1488
(+20) 100 418 9955
e-mail us
[email protected]

Working Hours

Sat–Thu 10:00am–4:30pm

Emergency Cases

Call us! (+20) 120 583 0835

Our Location

Inheritance Genomic Center, El-Basatin Sharkeya, El Basatin, Cairo, Egypt, 11728

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Amniotic Fluid Chromosomal Analysis (13,18 ,21, X&Y )