Health Concerns |
Popular Tests |
Bowel Health | |
Diabetes and Cholesterol Rapid | |
Kidney Health | |
Advanced Well Woman |
Health Concerns |
Popular Tests |
Bowel Health | |
Diabetes and Cholesterol Rapid | |
Kidney Health | |
Advanced Well Woman |
Our NIPT blood tests are safe and non-Invasive screening tests that use DNA found in your blood to detect chromosomal anomalies in your baby, and their gender, from the earliest weeks of your pregnancy.
Suitable for women of all ages, single or twin pregnancies, naturally conceived or through IVF.
This is the safest and easiest way to find out the gender or check the genetic health of your baby during pregnancy, with FREE genetic counselling provided if you receive a positive result for any health condition.
We provide a specialised testing kit to take with you to your appointment and a FREE pre-consultation on Karyo, Karyo Plus, and Complete Plus Tests.
See all our prenatal blood tests below. All NIPT Genetic Health tests offer free genetic counselling if required.
Find out the gender of your baby or babies from just 6 weeks of pregnancy. This test does not include checks for genetic health conditions.
£165
Check for the most common Trisomy disorders: Down Syndrome, Edwards Syndrome & Patau Syndrome.
£315
All conditions included in PrenatalSAFE 3 plus checks for Turner Syndrome, Klinefelter Syndrome & Jacobs Syndrome.
£375
All conditions included in PrenatalSAFE 5 plus checks on all chromosomes for aneuploidies, deletions & duplications.
£645
All conditions included in PrenatalSAFE Karyo, plus checks for 9 microdeletion syndromes including Prader-Willi, Angelman & DiGeorge Syndrome.
£795
Our most comprehensive NIPT test.
All conditions included in PrenatalSAFE Karyo Plus, as well as checks for 5 inherited genetic diseases and up to 50 De Novo diseases.
£1545
Our genetic health tests are called NIPT tests, or Non-Invasive Prenatal Tests. An NIPT is a blood test taken from the mother during pregnancy, using state of the art DNA technology to check whether the baby has high risks of certain chromosomal health conditions.
During pregnancy the placenta sheds cell free DNA (cfDNA) into the mother’s bloodstream. This means that the mother’s blood continues a mixture of your own DNA, and that of your baby’s placenta.
By extracting and evaluating the cfDNA in your blood, we can identify the risk to your baby of a range of health conditions and diseases.
This test is designed for women of at least 10 weeks of gestation (at the time of their blood draw appointment), who have had their pregnancy type (single or twin) previously confirmed by an ultrasound scan.
o Ongoing malignant tumour conditions
o Previous bone marrow or organ transplant, or stem cell therapy
o Recent blood transfusion (within the last 4 months)
o Mother affected by trisomy 21 or certain balanced translocation or mosaicism of T21, T18 or T13
o Immunotherapy (other than those required for IVF treatment (e.g. intravenous immunoglobulin – IVIg)
o Triplets or higher-order pregnancies
Call Us: 01225 444 144
The Blue Building, Stubbs Lane, Beckington BA11 6TE
Registration No. 12049669
Goodbody Clinic is a trading name of Goodbody Wellness Ltd, a subsidiary of Goodbody Health Ltd.