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VERACITY TEST

HOW IS THE VERACITY TEST REALIZED?

During pregnancy, fetal’s DNA passes through the placenta, enters the mother’s bloodstream, and circulates along with the mother’s DNA. The VERACITY test is a new generation non-invasive prenatal test that accurately measures and analyzes fetal DNA in maternal blood to detect the presence of fetal aneuploidy. The VERACITY test is valid for normal and twin pregnancies. The doctor or laboratory technician takes the mother’s blood sample and sends it to our state-of-the-art laboratories for analysis. The results are sent to your doctor within a few days.

WHY SHOULD WE CONSIDER THE VERACITY TEST?

High accuracy> 99% for autosomal aneuploidy.
Non-invasive – there is no risk of miscarriage, a test that only requires taking blood from the mother.
Available from the 10th week of pregnancy, and the result is obtained within a few days.

WHAT CAN THE VERACITY TEST DETECT?

AUTOSOMAL CHROMOSOPATIC ANEUPLOIDIES
Down Syndrome (Trizomy 21)
Edward Syndrome (Trizomy 18) Pata Syndrome (Trizomy 13)


ANEUPLOIDIES OF GENDER CHROMOSOMES

(Only in same-sex pregnancies) Tarner Syndrome (45 X) Triple Syndrome X (47 XXX) Klinefelter Syndrome (47 XXY) Jacobs Syndrome (47 XYY) (48 XXYY)

MICRODELETION

  • George Syndrome (22Q11.2)
  • Deletion Syndrome (1P36)
  • SMITH-MAGENIS SYNDROME (17P11.2) Volv-Hirschhorn Syndrome (4P16.3)


DEFINITION OF THE GENDER OF THE BABY

– WHAT CAN ANALYSIS VERACITY AND WHAT TYPE TO SELECT?
– VeraCITY Basic

Trisomy

Down Syndrome (Trisomy 21), extra copy of chromosome 21 (1/700) 2. Edwards Syndrome (Trisomy 18), extra copy of chromosome 18 (1/5000) 3. Patau Syndrome (Trisomy 13), extra copy of chromosome 13th (1 / 16,000).

VeraCITY PLUS

ANEUPLOIDIES OF GENDER CHROMOSOMES
Turner Syndrome (Monosomy X) – Lack of X chromosome (1 / 2,000 in female children) 2. Triple X syndrome (Trisomy X) – Excess X chromosome in female children (1 / 1,000 in female children ) 3. Klinefelter Syndrome (XXY) – Excess X chromosome in male children (1 / 1,000 for male children) Jacobs syndrome (XYY) – Excess Y chromosome in male children (1 / 1,000 for children male sex) 4.XYY Syndrome – Excess of X and Y chromosomes (1 / 17,000 for male children).

VeraCITY PREMIUM

MICRODELETION

Di George Syndrome (22Q11.2) – Missing part of chromosome 22, (1 / 1,000) 2.Deletion syndrome (1P36) – Missing part of chromosome 1, (1/5000) 3.SMITH-MAGENIS syndrome (17P11) .2) – Missing part of chromosome 17, (1 / 15.000) Volv-Hirschhorn syndrome (4P16.3) -Lack of chromosome part.

AvicenaKS Laboratory

AvicenaKS Laboratory is a center of excellence. Vision, perseverance, and innovation are what represents us. The professionalism and dedication of the doctors in Avicena Laboratory enable all patients specialized medical service in the highest standards that medicine offers today. The heart of our laboratory is the patients and their needs.