Nova Clinic is glad to offer their patients a genetic screening for fetal chromosomal mutations through the analysis of the mother’s blood sample with the help of next-generation sequencing (NGS) technique.
Non-invasive genetic test helps detect most wide-spread chromosomal pathologies:
- Down’s syndrome
- Edwards' syndrome
- Patau's syndrome
- Klinefelter's syndrome
- Turner's syndrome
A patient receives the geneticist’s medical conclusion as well as the results of the test.
Advantages of non-invasive prenatal test
There is no contact with an embryo’s membrane, which, otherwise, may cause miscarriages or other complications. A venous blood sample collected from a woman is quite enough to perform the test. All these are safe both for the mother and the fetus.
The non-invasive test uses fetal DNA, which, unlike an ultrasound and a biochemical screening, is a direct diagnostic technique with accuracy up to 99,9%. It should be also noted that the percentage of inaccurate (false-positive) results is inferior than 0,1% .
Indications
The test can be recommended to all pregnant women who want to obtain additional information on their babies’ health condition. However, the test is usually recommended to women running a high risk of having a baby with chromosomal mutations:
- when a women is over 35
- when a man is over 42
- ultrasound or a biochemical screening indicate to a high risk of developing a chromosomal pathology
- balanced chromosomal alteration has been found in one of the parents
Restrictions on a non-invasive prenatal diagnosis
- pregnancy term is less than 10 weeks
- multifetal pregnancy
- blood transfusion (over two recent years)
- organ transplant operations or treatment with stem cells
- oncological diseases
- IVF with donor egg cells
- surrogacy
Non-invasive prenatal diagnosis includes the following steps
- collection of a venous blood sample
- blood sample screening for fetal chromosomal pathologies
- calculation of an individual risk of having a baby with chromosomal mutations
- geneticist’s medical conclusion on the mother’s health condition
Non-invasive prenatal genetic test
Nova Clinic is glad to offer their patients a genetic screening for fetal chromosomal mutations through the analysis of the mother’s blood sample with the help of next-generation sequencing (NGS) technique.
Non-invasive genetic test helps detect most wide-spread chromosomal pathologies:
Down’s syndrome
Edwards' syndrome
Patau's syndrome
Klinefelter's syndrome
Turner's syndrome
A patient receives the geneticist’s medical conclusion as well as the results of the test.
Advantages of non-invasive prenatal test
Safety
There is no contact with an embryo’s membrane, which, otherwise, may cause miscarriages or other complications. A venous blood sample collected from a woman is quite enough to perform the test. All these are safe both for the mother and the fetus.
High accuracy
The non-invasive test uses fetal DNA, which, unlike an ultrasound and a biochemical screening, is a direct diagnostic technique with accuracy up to 99,9%. It should be also noted that the percentage of inaccurate (false-positive) results is inferior than 0,1% .
Indications
The test can be recommended to all pregnant women who want to obtain additional information on their babies’ health condition. However, the test is usually recommended to women running a high risk of having a baby with chromosomal mutations:
when a women is over 35
when a man is over 42
ultrasound or a biochemical screening indicate to a high risk of developing a chromosomal pathology
balanced chromosomal alteration has been found in one of the parents
Restrictions on a non-invasive prenatal diagnosis
pregnancy term is less than 10 weeks
multifetal pregnancy
blood transfusion (over two recent years)
organ transplant operations or treatment with stem cells
oncological diseases
IVF with donor egg cells
surrogacy
Non-invasive prenatal diagnosis includes the following steps
collection of a venous blood sample
blood sample screening for fetal chromosomal pathologies
calculation of an individual risk of having a baby with chromosomal mutations
geneticist’s medical conclusion on the mother’s health condition
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2023-11-02T12:39:53+03:00