• HIGHLY ACCURATE - detection rate
• SAFE - No risk of fetal miscarriage and Non-invasive test using a simple blood draw from the arm with no risk for the mother and the fetus
• FAST - Can be done from 10 weeks Results in 4-7 working days
• TRUSTED - Validated in three multi-centre studies using thousands of samples. Used by health professionals around the world.

• PrenatalSAFE 3  is a NIPT test done for the screening of aneuploidies such as Downs syndrome, Edwards syndrome, Patau syndrome 
• 30-minute Appointment with Qualified Health Professional
• 1 sample of blood taken from the arm of the mother
• Optional DNA sexing of Baby Optional Extra, 

• Safe, this test poses no risk for your baby.
• Quick and simple blood test drawn from the mother’s arms
• Our service includes the Harmony blood test and a scan, allowing you to see your baby, in the comfort of our first-class facilities.
• Developed in the USA by Ariosa Diagnostics, the Harmony Test is a non-invasive blood test for pregnant women from 10 weeks of pregnancy.
• It has a 99% detection rate for Down Syndrome and will also identify most cases of Edward Syndrome and Patau Syndrome

• Panorama: Next-generation NIPT. Panorama is a market-leading non-invasive prenatal screening test (NIPT) that reveals your baby’s risk for genetic disorders as early as 9 weeks. Panorama analyzes baby’s (placental) DNA through a simple blood draw from the mother’s arm. 

• The IONA® test is a safe non-invasive and accurate screening test for Downs Syndrome, Edwards’ Syndrome and Patau’s Syndrome. 
• We can offer this test at home to anyone who has had a scan to date the pregnancy.  The ideal time is around 10 weeks. 
• The test is more accurate than the standard combined test offered by the NHS as it uses DNA from the baby found in the mother’s blood to assess risk which the combined test does not.

Vistara screens for serious conditions across for 30 skeletal, cardiac and neurological disorders with a combined incidence of 1 in 600 

• This test screens for 5 common inherited recessive genetic disorders, such as Cystic Fibrosis, Beta-Thalassemia, Sickle cell anaemia, Deafness autosomal recessive type 1a and 1b.
• Allows detection of common inherited disorders within the foetus.
• Genes screened: CFTR, CX26 (GJB2), CX30 (GJB6), HBB .

Any Blood Tests (from £50.00) - please ring our clinic if you would like to know the price prior your appointment 

Most of the blood tests we offer are listed below however this list is not exhaustive. If you do not find what you are looking for or would like further information , please contact us for these blood test on 📞 07984572767 to speak with the Healthcare Professional would be happy to assist.

NB. Blood results require interpretation. All results should be interpreted by your regular health care professional / GP

• Horizon  Advanced DNA carrier screening (Pre-conception )  test for up to 274 autosomal recessive and X-linked genetic conditions
• Horizon^TMis a DNA screening test that provides information on patients´ chance of having a child with a genetic condition.
• Horizon´s technology provides comprehensive screening results for commonly screened conditions, like Cystic Fibrosis, Duchenne Muscular Dystrophy, Fragile X, Spinal Muscular Atrophy
• Knowing the carrier status of genetic conditions allows patients to make more informed reproductive decisions.

• Adventia CARRIER SCREENING test for up to 229 autosomal recessive and X-linked genetic conditions
• Adventia CARRIER SCREENING test is a DNA screening test that provides information on patients´ chance of having a child with a genetic condition.
• Adventia CARRIER SCREENING test provides a  comprehensive screening results for commonly screened conditions, like Cystic Fibrosis, Duchenne Muscular Dystrophy, Fragile X, Spinal Muscular Atrophy

• CONSULTATION (GENETIC)   -  £200.00

A consultation with one of our Medical Consultants or Genetic Counsellors.

• COLOR 30 CANCER TEST    -  £495.00

A simple saliva test to check up to 30 gene mutations (such as BRCA1 and 2) linked to higher risks of 8 common cancers  that impact risk for breast, ovarian, uterine, colon, melanoma, pancreatic, stomach, and prostate cancers.

• HIGHLY ACCURATE & SAFE 
• TARGETED TECHNOLOGY - By focusing only on the genetic changes tested, PreSENTIA is accurate and precise.
• HIGH READ DEPTH - PreSENTIA analyzes the locations of the genetic changes hundreds of times, making the test results more sensitive and reliable.
• TRUSTED - Validated in three multi-centre studies using thousands of samples. Used by health professionals around the world.

The Outlook newborn screening test can screen your baby for a range of genetic conditions likely to develop within their first few months of life. It gives you a clear picture of your baby’s predisposition to develop like 

• Lactose intolerance
• Coeliac disease
• Medication-induced deafness 
• Bitter taste

• Group B Streptococcus (GBS) is the most common cause of life-threatening infections in newborn babies in the UK. 

• Group B Strep (GBS) is a bacteria present in the vagina and bowel of around 20% of women in the UK.

• It does not cause harm or any health concerns in the women that carry it.