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Pre-Natal genetic screening testing service

Many fetal genetic diseases are caused by an abnormality in the number of chromosomes. Down’s syndrome is one of these common genetic diseases. The overall incidence is 1 in 700 live births, which increases significantly in mothers over 35 years old. In Hong Kong alone, there are approximately 80 cases of Down’s syndrome every year.

Pre-natal screening is the process used to identify the cause of a disease or illness by analyzing chromosome abnormality in the patients DNA. Karyotyping and fluorescent-PCR are two common methods used to screen for chromosomal aneuploidy.

  • Pre-Natal screening service: fluorescent-PCR

    Chromosomes carry the genetic instructions necessary for life. Humans have 46 chromosomes and inherit 23 from each parent. DNA-TECH Limited is the only private laboratory to offer fluorescent-PCR screening in Asia. Fluorescent-PCR allows rapid screening for fetal abnormalities. DNA-TECH focuses on screening 5 chromosome defects that account for over 95% of fetal chromosomal aneuploidy

    We focus on detecting the following conditions:
    Trisomy 21 V Down's syndrome
    Trisomy 18 V Edward's syndrome
    Trisomy 13 V Patau's syndrome
    X-aneuploidy and Y-aneuploidy

    How is the chromosomal aneuploidy test carried out?
    After consultation, your OG doctor will perform an amniocentesis. Amniocentesis should be performed after 16 weeks gestation to collect fetal cells for testing. Samples obtained will be sent for screening at our laboratory. Karyotyping and fluorescent-PCR are two common screening methods.

    Karyotyping fluorescent-PCR
    10 working days or more 1 working day
    Screen for all chromosomes Screen for chromosome 13, 18, 21, X, Y only ; Over 95% of fetal chromosomal aneuploidy

  • Karyotyping normally takes 2-3 weeks to determine the genetic health of the fetus. This can be a very stressful time for parents, as they may need to make very important decisions based on the test results. Fluorescent-PCR is a new technology that can screen the chromosomes causing 95% of fetal chromosomal aneuploidy within one day. This helps to relieve the stress and allows extra time for parents to make important decisions.

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