Diagnostics of Molecular Karyotype

Method:

Array CGH
(Array Comparative Genomic Hybridization)

Full name:

Sample Type:

Sample quantity:

Sample container:

15-18 weeks of fetal fluid

20 ml

Biomaterial container

- High-risk pregnant women who are at risk of miscarriage during ultrasound examination, fetal abnormalities,

developmental defects in internal organs, cleft palate and lip, etc.

- In the first three months, NT – the thickness of the nape of the neck is higher than normal indicators

when

- Repeated miscarriages, those with anomalous abortions

- Presence of an identified balanced translocation in either male or female

- The birth of children with mental and physical development in the family from the previous pregnancy

- When a suspicious chromosome is identified by fetal karyotype analysis or other

unless specified by methods

- The age of a pregnant woman is over 35

- Presence of chromosomal abnormality in abortion material from previous pregnancy

- Presence of chromosomal pathologies in close relatives