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The details are also securely saved on our fetal database so that we are able to monitor the growth of your baby during future scans.
With your permission, we'll send you information about our products and services based on what you're looking for via email, our apps, and our site.However, if you live in Northern Ireland, you'll need to pay to have it done privately.It assesses your risk of having a baby with a chromosomal abnormality such as Down's syndrome, Edwards' syndrome, and Patau’s syndrome.If you decide that one of these tests is the best option for you, you may need to pay to have it done at a private clinic.Non-invasive prenatal testing (NIPT): from 10 weeks NIPT screens for chromosomal abnormalities that may cause genetic conditions such as Down's syndrome, Edwards' syndrome and Patau’s syndrome.You can change your mind and withdraw your permission at any time.
Different countries may have different data-protection rules than your own.
The combined test also includes a blood test, which checks for the hormone human chorionic gonadotrophin (h CG), and pregnancy-associated plasma protein (PAPP-A). You'll have a nuchal translucency (NT) scan, and a blood test to analyse your levels of pregnancy-associated plasma protein (PAPP-A).
The results of the NT scan and the blood test are combined to determine how likely it is that you're expecting a baby with a chromosomal abnormality. The integrated test: first stage before 14 weeks; second stage between 15 weeks and 20 weeks Some clinics also offer the integrated test, which can assess your risk of having a baby with Down's syndrome or Edward's syndrome. The second stage happens between 15 weeks and 20 weeks.
Bear in mind that NIPT, the combined test and the integrated test can only assess your risk of having a baby with a chromosomal abnormality.
If your results show a high risk, you'll be offered a diagnostic test, such as chorionic villus sampling (CVS) or amniocentesis.
These tests are available on the NHS to people with a high-risk screening result, and will confirm whether your unborn baby has a genetic condition.