Blood Test (Price variable)
|Harmony Test , NIPT (from 10 weeks) £460|
|A non-invasive test that assess the risk for chromosome condition such as Down’s Syndrome (T21), Edward’s Syndrome (T18) , Patau Sundrome (T13) and includes optional analysis of foetal sex and sex chromosome (X,Y) conditions.
This test can also screen for the following sex chromosome abnormalities.
Turner Syndrome (Monosomy x) ; Triple x (XXX); Klinefelter Syndrome (XXY) and Jacob’s Syndrome (XYY).
Includes blood test and scan.
|Antenatal Blood tests|
|Antenatal blood screening, tumour markers, thyroid functions, hormones, women’s and men’s health screens.|
|IONA NIPT (£400)|
|IONA is a non-invasive prenatal test, that can be carried out as early as 10 weeks into a pregnancy on a small maternal blood sample.
Maternal blood sample contains a mixture of fetal and maternal circulating DNA. IONA directly measures the amount of this cell-free DNA and can detect small changes in the DNA ratio between the maternal and cell-free DNA when a fetal Trisomy 21, 18 or 13 is present.
This test measures the number of chromosome copies in the woman’s blood which can be related to conditions such as: Down’s Syndrome (T21); Edward’s Syndrome (T18) ; Patau’s Syndrome (T13).
If fetal sex determination is requested, the accuracy is greater than 99%.
A non-invasive test that assess the risk for chromosome conditions such as Down Syndrome (T21, Edwards Syndrome (T18), Patau Syndrome (T13) and sex chromosomes (optional).
|VISION+ 3 micro-deletion
A non-invasive test that assess the risk for chromosome conditions such as Down Syndrome (T21, Edwards Syndrome (T18), Patau Syndrome (T13) + Trisomy 9 (that causes spontaneous miscarriage, malformation, as well as mental deficiency), Trisomy 16 (that causes spontaneous miscarriage during the first trimester and has been shown to account 12% of chromosomally abnormal miscarriages) and 6 Microdeletion syndromes.