PLAN

Number

minutes

Price

Price for 1 minute

TRISOMY test


Down syndrome (trisomy 21)

Edwards syndrome (trisomy 18)

Patau syndrome (trisomy 13)

 

Prediction of fetal sex

TRISOMY test XY


Down syndrome (trisomy 21)

Edwards syndrome (trisomy 18)

Patau syndrome (trisomy 13)

 

Prediction of fetal sex

  

Turner syndrome (45 X)

Klinefelter syndrome (47 XXY)

XYY syndrome (47 XYY)

XXX syndrome (47 XXX)


TRISOMY test +


Down syndrome (trisomy 21)

Edwards syndrome (trisomy 18)

Patau syndrome (trisomy 13)

 

Prediction of fetal sex

 

Turner syndrome (45 X)

Klinefelter syndrome (47 XXY)

XYY syndrome (47 XYY)

XXX syndrome (47 XXX)

 

DiGeorge syndrome (22q11)

Prader-Willi and Angelman syndrome (15q11)

Cri-du-chat syndrome (5p15)

1p36 deletion syndrome


Wolf-Hirschhorn syndrome (4p16.3)


TRISOMY test Complete 


Screening of all 46 chromosomes of the fetus for detection of:

- changes in the number of whole chromosomes (trisomies, monosomies), sex chromosomes,

- changes in the number of one of the 46 chromosomes (duplications, deletions)

 

Prediction of fetal sex.

 

Advantages:

The price of the test includes validation of a positive result using GenomeScreen prenatal, the diagnostic test.


Following a resolution of the Ethics Committee of the Ministry of Health of the Slovak Republic, the Laboratory provides test results only upon completion of the 12th week of pregnancy.

Trisomy and its risks

Random cell division abnormalities may occur during egg maturation and in the early phases of egg fertilisation. If these processes lead ot an extra copy of one of the chromosomes, which means a particular chromosome occurs in three rather than two instances, the condition is called trisomy.

TRISOMY test

There is a certain amount of foetal DNA in maternal blood already in the early stages of pregnancy. Using a special screening laboratory test, it is possible to isolate this foetal DNA and analyse it to determine the risk of foetal trisomy (three identical chromosomes).

Consult your doctor

TRISOMY test (or any of its variants) is designed to exclude the presence of trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), and trisomy 13 (Patau syndrome) with a high degree of accuracy. If the mother-to-be wishes to know, the test can also determine the sex of her unborn baby.

Company TRISOMY test Ltd. meets the requirements of​ ISO 9001:2016.

Laboratories of TRISOMY test Ltd. are accredited according to ISO 15189:2012

and in analyses of samples unique bioinformatical tool accredited according to ISO 13485:2016 is being used.